Oxidation of Alcohols, Carbohydrates and Diols

Part of the Catalysis by Metal Complexes book series (CMCO, volume 34)


This is one of the most important classes of oxidation effected by Ru complexes, particularly by RuO4, [RuO4], [RuO4]2− and RuCl2(PPh3)3, though in fact most Ru oxidants effect these transformations. The chapter covers oxidation of primary alcohols to aldehydes (section 2.1), and to carboxylic acids (2.2), and of secondary alcohols to ketones (2.3). Oxidation of primary and secondary alcohol functionalities in carbohydrates (sugars) is dealt with in section 2.4, then oxidation of diols and polyols to lactones and acids (2.5). Finally there is a short section on miscellaneous alcohol oxidations in section 2.6.


Primary Alcohol Secondary Alcohol Cinnamyl Alcohol Carbohydrate Oxidation Allylic Alcohol 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


  1. 1.
    Berkowitz LM, Rylander PN (1958) J Am Chem Soc 80:6682–6684CrossRefGoogle Scholar
  2. 2.
    Parikh VM, Jones JKN (1965) Can J Chem 43:3452–3453CrossRefGoogle Scholar
  3. 3.
    Pagliaro M, Campestrini S, Ciriminna R (2005) Chem Soc Rev 34:837–845CrossRefGoogle Scholar
  4. 4.
    Che CM, Lau TC (2004) In: McCleverty JA, Meyer TJ (eds) Comprehensive coordination chemistry II, vol 5. Elsevier, Oxford, pp 733–847CrossRefGoogle Scholar
  5. 5.
    Arends IWCE, Kodama T, Sheldon RA (2004) In: Bruneau C, Dixneuf PH (eds) Topics organometallic chemistry, vol 11. Springer, Berlin, pp 277–320Google Scholar
  6. 6.
    Murahashi SI, Komiya N (2004) In: Baeckvall JE (ed) Modern oxidation methods. Wiley-VCH Verlag GmbH, Weinheim, pp 165–191Google Scholar
  7. 7.
    Rylander PN (1975) Organic syntheses with noble metal catalysts. Academic Press, New York, pp 133–144Google Scholar
  8. 8.
    Ahrends IWCE, Sheldon RA (2004). In: Bäckvall JE (ed) Modern oxidation methods. Wiley-Verlag GmbH, Weinheim, pp 83–118Google Scholar
  9. 9.
    Murahashi SI, Komiya N (2004) In: Murahashi SI (ed) Ruthenium in organic synthesis. Wiley-VCH, Weinheim, pp 53–93CrossRefGoogle Scholar
  10. 10.
    Sheldon RA, Arends IWCE (2003) In: Simandi LI (ed) Advances in catalytic deactivation of dioxygen by metal complexes. Kluwer, Dordrecht, The Netherlands, pp 123–155Google Scholar
  11. 11.
    Murahashi SI, Komiya N (2000) In: Meunier B (ed) Biomimetic oxidations catalysed by transition metal complexes. Imperial College Press, London, pp 563–611CrossRefGoogle Scholar
  12. 12.
    Friedrich HB (1999) Platinum Metals Rev 43:94–102Google Scholar
  13. 13.
    Murahashi SI, Naota T (1996) Russ J Org Chem (Engl Transl) 32:203–213Google Scholar
  14. 14.
    Ley SV, Norman J, Griffith WP, Marsden SP (1994) Synthesis 639–666Google Scholar
  15. 15.
    Murahashi SI, Naota T (1994) Adv Met-Org Chem 3:225–253Google Scholar
  16. 16.
    Griffith WP, Ley SV (1990) Aldrichim Acta 23:13–19Google Scholar
  17. 17.
    Mimoun H, Wilkinson G, Gillard RD, McCleverty JA (1987) Comprehensive coordination chemistry, vol 6. Pergamon Press, Oxford, pp 317–410Google Scholar
  18. 18.
    Courtney JL (1986) In: Mijs WJ, de Jonge CRHI (eds) Organic syntheses by oxidation with metal compounds. Plenum Press, New York, pp 445–467CrossRefGoogle Scholar
  19. 19.
    Gore ES (1983) Platinum Metals Rev 27:111–125Google Scholar
  20. 20.
    Lee DG, van der Engh M (1973) In: Trahanowsky WS (ed) Oxidation in organic chemistry, part B. Academic Press, New York, pp 177–227CrossRefGoogle Scholar
  21. 21.
    Keene FR (1999) Coord Chem Rev 187:121–149CrossRefGoogle Scholar
  22. 22.
    Farmer V, Welton T (2002) Green Chem 4:97–102CrossRefGoogle Scholar
  23. 23.
    Ley SV, Ramarao C, Smith MD (2001) Chem Commun 2278–2279Google Scholar
  24. 24.
    Rajendran S, Trivedi DC (1995) Synthesis 153–154Google Scholar
  25. 25.
    Yamaoka H, Moriya N, Ikunaka M (2004) Org Process Res Dev 8:931–938CrossRefGoogle Scholar
  26. 26.
    Pârvulescu V, Vass M, Luca C (1999) Rev Roum Chim 44:361–368Google Scholar
  27. 27.
    Hinzen B, Lenz R, Ley SV (1998) Synthesis 977–979Google Scholar
  28. 28.
    Lenz R, Ley SV (1997) J Chem Soc Perkin Trans 1:1907–1908Google Scholar
  29. 29.
    Dengel AC, Griffith WP, El-Hendawy AM, Jolliffe JM (1990) Polyhedron 9:1751–1756CrossRefGoogle Scholar
  30. 30.
    Kim KS, Kim SJ, Song YH, Hahn CS (1987) Synthesis 1017–1018Google Scholar
  31. 31.
    Griffith WP, Ley SV, Whitcombe GP, White AD (1987) J Chem Soc Chem Commun 1625–1627Google Scholar
  32. 32.
    Kanemoto S, Tomioka H, Oshima K, Nozaki H (1986) Bull Chem Soc Jpn 59:105–108CrossRefGoogle Scholar
  33. 33.
    Torii S, Inokuchi T, Sugiura T (1986) J Org Chem 51:155–166CrossRefGoogle Scholar
  34. 34.
    Caputo JA, Fuchs R (1967) Tetrahedron Lett 4729–4731Google Scholar
  35. 35.
    Ciriminna R, Pagliaro M (2003) Chem Eur J 9:5067–5073CrossRefGoogle Scholar
  36. 36.
    Dijksman A, Ahrends IWCE, Sheldon RA (2001) Platinum Metals Rev 45:15–19Google Scholar
  37. 37.
    Dijksman A, Marino-González A, Mairata i Payeras A, Arends IWCE, Sheldon RA (2001) J Am Chem Soc 123:6826–6833CrossRefGoogle Scholar
  38. 38.
    Dijksman A, Arends IWCE, Sheldon RA (1999) Chem Commun 1591–1592Google Scholar
  39. 39.
    Tsuji Y, Ohta T, Ido T, Minbu H, Watanabe Y (1984) J Organomet Chem 270:333–341CrossRefGoogle Scholar
  40. 40.
    Green G, Griffith WP, Hollinshead DM, Ley SV, Schröder M (1984) J Chem Soc Perkin Trans 1:681–686Google Scholar
  41. 41.
    Sharpless KB, Akashi K, Oshima K (1976) Tetrahedron Lett 29:2503–2506CrossRefGoogle Scholar
  42. 42.
    Ley SV, Ramarao C (2002) In: Paquette LA (ed) Electronic encyclopedia of reagents for organic synthesis. Wiley, Chichester, pp
  43. 43.
    Langer P (2000) J Prakt Chem 342:728–730CrossRefGoogle Scholar
  44. 44.
    Ley SV, Baxendale IR, Bream RN, Jackson PS, Leach AG, Longbottom DA, Nesi M, Scott JS, Storer RI, Taylor SJ (2000) J Chem Soc Perkin Trans 1:3815–4193CrossRefGoogle Scholar
  45. 45.
    Ley SV, Norman J (1995) In: Paquette LA (ed) Encyclopedia of reagents for organic synthesis, vol 7. Wiley, Chichester, pp 4827–4830Google Scholar
  46. 46.
    Bloch R, Brillet C (1991) Synlett 829–830Google Scholar
  47. 47.
    Hitchcock SA, Pattenden G (1992) Tetrahedron Lett 33:4843–4846CrossRefGoogle Scholar
  48. 48.
    Ryall RP, Silverman RB (1990) Synth Commun 20:431–438CrossRefGoogle Scholar
  49. 49.
    Xiao X, Sen SE, Prestwich GD (1990) Tetrahedron Lett 31:2097–2100CrossRefGoogle Scholar
  50. 50.
    Kim G, Chu-Moyer MY, Danishefsky SJ (1990) J Am Chem Soc 112:2003–2005CrossRefGoogle Scholar
  51. 51.
    Nakamura T, Tsuboi K, Oshida M, Nomura T, Nakazaki A, Kobayashi S (2009) Tetrahedron Lett 50:2835–2839CrossRefGoogle Scholar
  52. 52.
    Bates RW, Fernández-Megía E, Ley SV, Rück-Braun K, Tilbrook DMG (1999) J Chem Soc Perkin Trans 1:1917–1925CrossRefGoogle Scholar
  53. 53.
    Baldwin JE, Adlington RM, Mitchell MB (1993) J Chem Soc Chem Commun 1332–1335Google Scholar
  54. 54.
    Tokoroyama T, Kotsuji Y, Matsuyama H, Shimura T, Yokotani K, Fukuyama Y (1990) J Chem Soc Perkin Trans 1:1745–1752CrossRefGoogle Scholar
  55. 55.
    Hu Y, Ziffer H (1991) J Labelled Compd Rad 29:1293–1299CrossRefGoogle Scholar
  56. 56.
    Baldwin JE, Adlington RM, Marquess DG, Pitt AR, Porter MJ, Russell AT (1996) Tetrahedron 52:2537–2556CrossRefGoogle Scholar
  57. 57.
    Baldwin JE, Adlington RM, Marquess DG, Pitt AR, Porter MJ, Russell AT (1996) Tetrahedron 52:2515–2536CrossRefGoogle Scholar
  58. 58.
    Rychnovsky SD, Rodriguez C (1992) J Org Chem 57:4793–4795CrossRefGoogle Scholar
  59. 59.
    Guanti G, Banfi L, Narisano E, Riva R (1992) Tetrahedron Lett 33:2221–2222CrossRefGoogle Scholar
  60. 60.
    Guanti G, Banfi L, Narisano E, Thea S (1992) Synlett 311–312Google Scholar
  61. 61.
    Robl JA, Duncan LA, Pluscec J, Karanewsky DS, Gordon EM, Ciosek CP, Rich LC, Dehmel VC, Slusarchyk DA, Harrity TW, O’Brien KA (1991) J Med Chem 34:2804–2815CrossRefGoogle Scholar
  62. 62.
    Tuck SF, Robinson CH, Silverton JV (1991) J Org Chem 56:1260–1266CrossRefGoogle Scholar
  63. 63.
    Shimazaki M, Hara H, Suzuki K (1989) Tetrahedron Lett 30:5443–5446CrossRefGoogle Scholar
  64. 64.
    Oliver SF, Högenauer K, Simic O, Antonello A, Smith MD, Ley SV (2003) Angew Chem Int Edit 42:5996–6000CrossRefGoogle Scholar
  65. 65.
    Paquette LA, Tae J, Branan BM, Bolin DG, Eisenberg SWE (2000) J Org Chem 65:9172–9179CrossRefGoogle Scholar
  66. 66.
    Mukaiyama T, Shiina I, Iwadare H, Saitoh M, Nishimura T, Ohkawa N, Sakoh H, Nishimura K, Tani Y, Hasegawa M, Yamada K, Saitoh K (1999) Chem Eur J 5:121–161CrossRefGoogle Scholar
  67. 67.
    Haunert F, Bolli MH, Hinzen B, Ley SV (1998) J Chem Soc Perkin Trans 1:2235–2237CrossRefGoogle Scholar
  68. 68.
    Ley SV, Bolli MH, Hinzen B, Gervois AG, Hall BJ (1998) J Chem Soc Perkin Trans 1:2239–2241CrossRefGoogle Scholar
  69. 69.
    Baxendale IR, Deeley J, Griffiths-Jones CM, Ley SV, Saaby S, Tranmer GK (2006) Chem Commun 2566–2568Google Scholar
  70. 70.
    Bleloch A, Johnson BFG, Ley SV, Shephard DS, Thomas AW (1999) Chem Commun 1907–1908Google Scholar
  71. 71.
    Hinzen B, Ley SV (1997) J Chem Soc Perkin Trans 1:1907–1908CrossRefGoogle Scholar
  72. 72.
    Campestrini S, Carraro M, Ciriminna R, Pagliaro M, Tonellato U (2004) Tetrahedron Lett 45:7283–7286CrossRefGoogle Scholar
  73. 73.
    Brown DS, Kerr WJ, Lindsay DM, Pike KG, Ratcliffe PD (2001) Synlett 1257–1259Google Scholar
  74. 74.
    Coleman KS, Lorber CY, Osborn JA (1998) Eur J Inorg Chem 1673–1675Google Scholar
  75. 75.
    Markó IE, Giles PR, Tsukazaki M, Chellé-Regnaut I, Urch CJ, Brown SM (1997) J Am Chem Soc 119:12661–12662CrossRefGoogle Scholar
  76. 76.
    Cao E, Motherwell WB, Gavriilidis A (2006) Chem Eng Technol 29:1372–1375CrossRefGoogle Scholar
  77. 77.
    Smith TR, Clark AJ, Clarkson GJ, Taylor PC, Marsh A (2006) Org Biomol Chem 4:4186–4192CrossRefGoogle Scholar
  78. 78.
    Enders D, Barbion J (2008) Chem Eur J 14:2842–2849CrossRefGoogle Scholar
  79. 79.
    Guo J, Duffy KJ, Stevens KL, Dalko PI, Roth RM, Hayward MM, Kishi Y (1998) Angew Chem Int Edit 37:187–191CrossRefGoogle Scholar
  80. 80.
    Petri A, Bayer A, Meier ME (2004) Angew Chem Int Edit 43:5821–5823CrossRefGoogle Scholar
  81. 81.
    Ley SV, Armstrong A, Díez-Martín D, Ford MJ, Grice P, Knight JG, Kolb HC, Madin A, Marby CA, Mukherjee S, Shaw AN, Slawin AMZ, Vile S, White AD, Williams DJ, Woods M (1991) J Chem Soc Perkin Trans 1:667–692CrossRefGoogle Scholar
  82. 82.
    Díez-Martín D, Grice P, Kolb HC, Ley SV, Madin A (1990) Synlett 326–328Google Scholar
  83. 83.
    Sunazuka T, Handa M, Nagai K, Shirahata T, Harigaya Y, Otoguro K, Kuwajima I, Ōmura S (2004) Tetrahedron 60:7845–7859CrossRefGoogle Scholar
  84. 84.
    Crimmins MT, Brown BH, Plake HR (2006) J Am Chem Soc 128:1371–1378CrossRefGoogle Scholar
  85. 85.
    Nagamitsu T, Takano D, Fukuda T, Otoguro K, Kuwajima I, Harigaya Y, Ōmura S (2004) Org Lett 6:1865–1867CrossRefGoogle Scholar
  86. 86.
    Kadota I, Takamura H, Nishii H, Yamamoto Y (2005) J Am Chem Soc 127:9246–9250CrossRefGoogle Scholar
  87. 87.
    Nicolaou KC, Gunzner JL, Shi GQ, Agrios KA, Gärtner P, Yang Z (1999) Chem Eur J 5:646–658CrossRefGoogle Scholar
  88. 88.
    White JD, Hansen JD (2005) J Org Chem 70:1963–1977CrossRefGoogle Scholar
  89. 89.
    Shiina I, Takasuna Y, Suzuki R, Oshiumi H, Komiyama Y, Hitomi S, Fukui H (2006) Org Lett 8:5279–5282CrossRefGoogle Scholar
  90. 90.
    Sato K, Sasaki M (2007) Angew Chem Int Edit 46:2518–2522CrossRefGoogle Scholar
  91. 91.
    Fuwa H, Kainuma N, Tachibana K, Tsukano C, Satake M, Sasaki M (2004) Chem Eur J 10:4894–4909CrossRefGoogle Scholar
  92. 92.
    Tsukano C, Ebine M, Sasaki M (2005) J Am Chem Soc 127:4326–4335CrossRefGoogle Scholar
  93. 93.
    Nattrass GL, Díez E, McLachlan MM, Dixon DJ, Ley SV (2006) Angew Chem Int Edit 44:580–584Google Scholar
  94. 94.
    Williams DR, Walsh MJ, Miller NA (2009) J Am Chem Soc 131:9038–9045CrossRefGoogle Scholar
  95. 95.
    Hadfield JA, McGown AT, Butler J (2000) Molecules 5:82–88CrossRefGoogle Scholar
  96. 96.
    Shimada K, Kaburagi Y, Fukuyama T (2003) J Am Chem Soc 125:4048–4049CrossRefGoogle Scholar
  97. 97.
    Ley SV, Madin A, Monck NJT (1993) Tetrahedron Lett 34:7479–7482CrossRefGoogle Scholar
  98. 98.
    Ley SV, Anthony NJ, Armstrong A, Brasca MG, Clarke T, Culshaw D, Greck C, Grice P, Jones B, Lygo B, Madin A, Sheppard RN, Slawin AMZ, Williams DJ (1989) Tetrahedron 45:7161–7194CrossRefGoogle Scholar
  99. 99.
    Miyashita M, Sasaki M, Hattori I, Sakai M, Tanino K (2004) Science 305:495–498CrossRefGoogle Scholar
  100. 100.
    Blackburn TJ, Helliwell M, Kilner MJ, Lee ATL, Thomas EJ (2009) Tetrahedron Lett 50:3550–3554CrossRefGoogle Scholar
  101. 101.
    Sellars JD, Steel PG (2006) Org Biomol Chem 4:3223–3224CrossRefGoogle Scholar
  102. 102.
    Díez-Martín D, Kotecha NR, Ley SV, Mantegani S, Menéndez JC, Organ HM, White AD (1992) Tetrahedron 37:7899–7938CrossRefGoogle Scholar
  103. 103.
    Kotecha NR, Ley SV, Mantegani S (1992) Synlett 395–400Google Scholar
  104. 104.
    Herb C, Bayer A, Maier ME (2004) Chem Eur J 10:5649–5660CrossRefGoogle Scholar
  105. 105.
    Nicolaou KC, Xu JY, Kim S, Pfefferkorn J, Ohshima T, Vourloumis D, Hosokawa S (1998) J Am Chem Soc 120:8661–8673CrossRefGoogle Scholar
  106. 106.
    Magnin-Lachau M, Tan Z, Negishi E-I (2004) Org Lett 6:1425–1427CrossRefGoogle Scholar
  107. 107.
    Hori K, Hikage N, Inagaki A, Mori S, Nomura K, Yoshii E (1992) J Org Chem 57:2888–2902CrossRefGoogle Scholar
  108. 108.
    Takeda K, Kawanishi E, Nakamura H, Yoshii E (1991) Tetrahedron Lett 32:4925–4928CrossRefGoogle Scholar
  109. 109.
    Ley SV, Humphries AC, Eick H, Downham R, Ross AR, Boyce RJ, Pavey JBJ, Pietruszka J (1998) J Chem Soc Perkin Trans 1:3907–3911CrossRefGoogle Scholar
  110. 110.
    Schinzer D, Schulz C, Krug O (2004) Synlett 15:2689–2692CrossRefGoogle Scholar
  111. 111.
    Queneau Y, Krol WJ, Bornmann WG, Danishefsky SJ (1992) J Org Chem 57:4043–4047CrossRefGoogle Scholar
  112. 112.
    Ley SV, Antonello A, Balskus EP, Booth DT, Christensen SB, Cleator E, Gold H, Högenauer K, Hünger U, Myers RM, Oliver SF, Simic O, Smith MD, Søhoel H, Woodford AJA (2004) Proc Natl Acad Sci USA 101:12073–12078CrossRefGoogle Scholar
  113. 113.
    Ley SV, Brown DS, Clase JA, Fairbanks AJ, Lennon IC, Osborn HML, Stokes ESE, Wadsworth DJ (1998) J Chem Soc Perkin Trans 1:2259–2276CrossRefGoogle Scholar
  114. 114.
    Ley SV, Maw GN, Trudell ML (1990) Tetrahedron Lett 31:5521–5524CrossRefGoogle Scholar
  115. 115.
    Baldwin JE, Vollmer HR, Lee V (1999) Tetrahedron Lett 40:5401–5404CrossRefGoogle Scholar
  116. 116.
    Ley SV, Schucht O, Thomas AW, Murray PJ (1999) J Chem Soc Perkin Trans 1:1251–1252CrossRefGoogle Scholar
  117. 117.
    Habermann J, Scott JS (1999) J Chem Soc Perkin Trans 1:1253–1255CrossRefGoogle Scholar
  118. 118.
    Storer RI, Takemoto T, Jackson PS, Brown DS, Baxendale IR, Ley SV (2004) Chem Eur J 10:2529–2547CrossRefGoogle Scholar
  119. 119.
    Tandon PK, Baboo R, Singh AK, Gayatri K (2006) Appl Organomet Chem 20:20–23Google Scholar
  120. 120.
    Bailey AJ, Cother LD, Griffith WP, Hankin DM (1995) Transit Metal Chem 20:590–594CrossRefGoogle Scholar
  121. 121.
    Bailey AJ, Griffith WP, Mostafa SI, Sherwood PA (1993) Inorg Chem 32:268–271CrossRefGoogle Scholar
  122. 122.
    Schröder M, Griffith WP (1979) J Chem Soc Chem Commun 58–59Google Scholar
  123. 123.
    Chang JM, Sharpless KB (1985) J Org Chem 50:1560–1563CrossRefGoogle Scholar
  124. 124.
    Carlsen PHJ, Katsuki T, Martin VS, Sharpless KB (1981) J Org Chem 46:3936–3938CrossRefGoogle Scholar
  125. 125.
    Falck JR, Mekonnen B, Yu J, Lai JY (1996) J Am Chem Soc 118:6096–6097CrossRefGoogle Scholar
  126. 126.
    Corey EJ, Danheiser RL, Chandrasekaran S, Keck GE, Gopalan B, Larsen SD, Siret P, Gras JL (1978) J Am Chem Soc 100:8034–8036CrossRefGoogle Scholar
  127. 127.
    ter Horst B, Feringa BL, Minnaard AJ (2007) Chem Commun 5:489–491CrossRefGoogle Scholar
  128. 128.
    Bower JF, Riis-Johannessen T, Szeto P, Whitehead AJ, Gallagher T (2007) Chem Commun 7:728–730CrossRefGoogle Scholar
  129. 129.
    Still WC, Ohmizu H (1981) J Org Chem 46:5244–5246CrossRefGoogle Scholar
  130. 130.
    Brittain DEA, Griffiths-Jones CM, Linder MR, Smith MD, McCusker C, Barlow JS, Akiyama R, Yasuda K, Ley SV (2005) Angew Chem Int Edit 44:2732–2737CrossRefGoogle Scholar
  131. 131.
    Crimmins MT, Vanier GS (2006) Org Lett 8:2887–2890CrossRefGoogle Scholar
  132. 132.
    El-Hendawy AM, El-Shahawi MS (1989) Polyhedron 8:2813–2816CrossRefGoogle Scholar
  133. 133.
    Yamamoto Y, Suzuki H, Moro-oka Y (1985) Tetrahedron Lett 26:2107–2108CrossRefGoogle Scholar
  134. 134.
    Cheng SYS, Rajapakse N, Rettig RJ, James BR (1994) J Chem Soc Chem Commun 2669–2670Google Scholar
  135. 135.
    Bressan M, Forti L, Ghelfi F, Morvillo A (1993) J Mol Catal 79:85–93CrossRefGoogle Scholar
  136. 136.
    Wong KY, Lee WO, Che CM, Anson FC (1991) J Electroanal Chem 319:207–216CrossRefGoogle Scholar
  137. 137.
    Yam VWW, Che CM, Tong WT (1988) J Chem Soc Chem Commun 100–102Google Scholar
  138. 138.
    Corey EJ, Casanova J, Vatakencherry PA, Winter R (1963) J Am Chem Soc 85:169–173CrossRefGoogle Scholar
  139. 139.
    Nakata H (1963) Tetrahedron 19:1959–1963CrossRefGoogle Scholar
  140. 140.
    Nakamura Y, Egami H, Matsumoto K, Uchida T, Katsuki T (2007) Tetrahedron 63:6383–6387CrossRefGoogle Scholar
  141. 141.
    Mills A, Holland C (1995) Ultrason Sonochem 2:S33–S38CrossRefGoogle Scholar
  142. 142.
    Giddings S, Mills A (1988) J Org Chem 53:1103–1107CrossRefGoogle Scholar
  143. 143.
    Givens RS, Rademacher DR (1974) J Med Chem 17:457–459CrossRefGoogle Scholar
  144. 144.
    Tse MK, Bhor S, Klawonn M, Anilkumar G, Jiao H, Spannenberg A, Döbler C, Mägerlein W, Hugl H, Beller M (2006) Chem Eur J 12:1875–1888CrossRefGoogle Scholar
  145. 145.
    Ooi HC, Marcuccio SM, Jackson WR, O’Keefe DF (1999) Aust J Chem 52:1127–1130CrossRefGoogle Scholar
  146. 146.
    Sobti A, Sulikowski GA (1994) Tetrahedron Lett 35:3661–3664CrossRefGoogle Scholar
  147. 147.
    Taylor EC, Ahmed Z (1991) J Org Chem 56:5443–5445CrossRefGoogle Scholar
  148. 148.
    Piers E, Roberge JY (1991) Tetrahedron Lett 32:5219–5222CrossRefGoogle Scholar
  149. 149.
    Romeyke Y, Keller M, Kluge H, Grabley S, Hammann P (1991) Tetrahedron 47:3335–3346CrossRefGoogle Scholar
  150. 150.
    Collins S, Hong Y, Kataoka M, Nguyen T (1990) J Org Chem 55:3395–3398CrossRefGoogle Scholar
  151. 151.
    Collins S, Hong Y, Taylor NJ (1990) Organometallics 9:2695–2703CrossRefGoogle Scholar
  152. 152.
    Andrews SP, Ball M, Wierschem F, Cleator E, Oliver S, Högenauer K, Simic O, Antonello A, Hünger U, Smith MD, Ley SV (2007) Chem Eur J 13:5688–5712CrossRefGoogle Scholar
  153. 153.
    Andrews SP, Tait MM, Ball M, Ley SV (2007) Org Biomol Chem 5:1427–1426CrossRefGoogle Scholar
  154. 154.
    Ciriminna R, Campestrini S, Carraro M, Pagliaro M (2005) Adv Funct Mater 15:846–850CrossRefGoogle Scholar
  155. 155.
    Szewczyk K, Banaszek A (2000) Pol J Chem 74:1275–1281Google Scholar
  156. 156.
    Tony KJ, Mahadevan V, Rajaram J, Swamy CS (1997) React Kinet Catal Lett 62:105–116CrossRefGoogle Scholar
  157. 157.
    Desmaële D, Champion N (1992) Tetrahedron Lett 33:4447–4450CrossRefGoogle Scholar
  158. 158.
    Miranda Moreno MJS, Sá e Melo ML, Campos Neves AS (1991) Tetrahedron Lett 32:3201–3204CrossRefGoogle Scholar
  159. 159.
    Marshall JA, Robinson ED, Lebreton J (1990) J Org Chem 55:227–239CrossRefGoogle Scholar
  160. 160.
    Ley SV, Smith SC, Woodward PR (1992) Tetrahedron 48:1145–1174CrossRefGoogle Scholar
  161. 161.
    Carless HAJ, Malik SS (1992) Tetrahedron Asymm 3:1135–1138CrossRefGoogle Scholar
  162. 162.
    Ninan A, Sainsbury M (1992) Tetrahedron 48:6709–6716CrossRefGoogle Scholar
  163. 163.
    Chang S, Lee M, Ko S, Lee PH (2002) Synth Commun 32:1279–1284CrossRefGoogle Scholar
  164. 164.
    Wolfson A, Yehuda C, Shakin O, Tavor D (2006) Lett Org Chem 3:107–110CrossRefGoogle Scholar
  165. 165.
    Griffith WP (1992) Chem Soc Rev 21:179–185CrossRefGoogle Scholar
  166. 166.
    Fleitz F, Lyle TA, Zheng N, Armstrong JD, Volante RP (2000) Synth Commun 30:3171–3180CrossRefGoogle Scholar
  167. 167.
    Armstrong A, Ley SV, Madin A, Mukherjee S (1990) Synlett 6:328–330CrossRefGoogle Scholar
  168. 168.
    Mushti CS, Kim J-H, Corey EJ (2006) J Am Chem Soc 128:14050–14052CrossRefGoogle Scholar
  169. 169.
    Colby EA, O’Brien KC, Jamison TF (2005) J Am Chem Soc 127:4297–4307CrossRefGoogle Scholar
  170. 170.
    Shimokawa J, Ishiwata T, Shirai K, Koshino H, Tanatani A, Nakata T, Hashimoto Y, Nagasawa K (2005) Chem Eur J 11:6878–6888CrossRefGoogle Scholar
  171. 171.
    Moisan L, Thuéry P, Nicolas M, Doris E, Rousseau B (2006) Angew Chem Int Edit 45:5334–5336CrossRefGoogle Scholar
  172. 172.
    Tokunaga Y, Yagihashi M, Ihara M, Fukumoto K (1995) J Chem Soc Chem Commun 955–956Google Scholar
  173. 173.
    Fenster MDB, Dake GR (2005) Chem Eur J 11:639–649CrossRefGoogle Scholar
  174. 174.
    Trudeau S, Morken JP (2005) Org Lett 7:5465–5468CrossRefGoogle Scholar
  175. 175.
    Pearson WH, Lee IY, Mi Y, Stoy P (2004) J Org Chem 69:9109–9122CrossRefGoogle Scholar
  176. 176.
    Dixon DJ, Ley SV, Reynolds DJ (2000) Angew Chem Int Edit 39:3622–3626CrossRefGoogle Scholar
  177. 177.
    Shoji M, Akiyama N, Koichi T, Lash LL, Sanders JM, Swanson GT, Sakai R, Shimamoto K, Oikawa M, Sasaki M (2006) J Org Chem 71:5208–5220CrossRefGoogle Scholar
  178. 178.
    Takahashi S, Hishinuma N, Koshino H, Nakata T (2005) J Org Chem 70:10162–10165CrossRefGoogle Scholar
  179. 179.
    White JD, Kuntiyong P, Lee TH (2006) Org Lett 8:6039–6042CrossRefGoogle Scholar
  180. 180.
    McKay C, Simpson TJ, Willis CL, Forrest AK, O’Hamon PJ (2000) Chem Commun 1109–1110Google Scholar
  181. 181.
    Ley SV, Tackett MN, Maddess ML, Anderson JC, Brennan PE, Cappi MW, Heer JP, Helgen C, Kori M, Kouklovsky C, Marsden SP, Norman J, Osborn DP, Palomero MA, Pavey JBJ, Pinel C, Robinson LA, Schnaubelt J, Scott JS, Spilling CD, Watanabe H, Wesson KE, Willis MC (2009) Chem Eur J 15:2874–2914CrossRefGoogle Scholar
  182. 182.
    Maddess ML, Tackett MN, Watanabe H, Brennan PE, Spilling CD, Scott JS, Osborn DP, Ley SV (2007) Angew Chem Int Edit 46:591–597CrossRefGoogle Scholar
  183. 183.
    Wender PA, Jesudason CD, Nakahira H, Tamura N, Tebbe AL, Ueno Y (1997) J Am Chem Soc 119:12976–12977CrossRefGoogle Scholar
  184. 184.
    Jiang Y, Hong J, Burke SD (2004) Org Lett 6:1445–1448CrossRefGoogle Scholar
  185. 185.
    Robinson JE, Brimble MA (2005) Chem Commun 1560–1562Google Scholar
  186. 186.
    Jasper C, Adibekian A, Busch T, Quitschalle M, Wittenberg R, Kirschning A (2006) Chem Eur J 12:8719–8734CrossRefGoogle Scholar
  187. 187.
    Tomooka K, Kikuchi M, Igawa K, Suzuki M, Keong PH, Nakai T (2000) Angew Chem Int Edit 39:4502–4505CrossRefGoogle Scholar
  188. 188.
    Yokokawa F, Hamada Y, Shioiri T (1996) Chem Commun 871–872Google Scholar
  189. 189.
    Hu Y, Ziffer H, Li G, Yeh HJC (1992) Bioinorg Chem 20:148–154Google Scholar
  190. 190.
    Cywin CL, Kallmerten J (1991) J Nat Prod 54:1664–1667CrossRefGoogle Scholar
  191. 191.
    Yoshimitsu T, Sasaki S, Arano Y, Nagaoka H (2004) J Org Chem 69:9262–9268CrossRefGoogle Scholar
  192. 192.
    Boyer A, Veitch GE, Beckmann E, Ley SV (2009) Angew Chem Int Edit 121:1343–1346CrossRefGoogle Scholar
  193. 193.
    Veitch GE, Boyer A, Ley SV (2008) Angew Chem Int Edit 47:9402–9429CrossRefGoogle Scholar
  194. 194.
    Veitch GE, Beckmann E, Boyer A, Maslen SL, Ley SV (2007) Angew Chem Int Edit 46:591–597CrossRefGoogle Scholar
  195. 195.
    Anderson JC, Ley SV, Santafianos D, Sheppard RN (1991) Tetrahedron 47:6813–6850CrossRefGoogle Scholar
  196. 196.
    Anderson JC, Ley SV (1990) Tetrahedron Lett 31:431–432CrossRefGoogle Scholar
  197. 197.
    Takahashi K, Matsumura T, Ishihara J, Hatakeyama S (2007) Chem Commun 40:4158–4160CrossRefGoogle Scholar
  198. 198.
    Baldwin JE, Adlington RM, Mitchell MB (1995) Tetrahedron 51(17):5193–5206CrossRefGoogle Scholar
  199. 199.
    Tate EW, Dixon DJ, Ley SV (2006) Org Biomol Chem 4:1698–1706CrossRefGoogle Scholar
  200. 200.
    Dixon DJ, Ley SV, Tate EW (1998) J Chem Soc Perkin Trans 1:3125–3126CrossRefGoogle Scholar
  201. 201.
    Gopal H, Adams T, Moriarty RM (1972) Tetrahedron 28:4259–4266CrossRefGoogle Scholar
  202. 202.
    Moriarty RM, Gopal H, Adams T (1970) Tetrahedron Lett 4003–4006Google Scholar
  203. 203.
    Ramey KC, Lini DC, Moriarty RM, Gopal H, Welsh HG (1967) J Am Chem Soc 89:2401–2408CrossRefGoogle Scholar
  204. 204.
    Murahashi SI, Naota T (1993) Synthesis 4:433–440CrossRefGoogle Scholar
  205. 205.
    Tanaka M, Kobayashi TA, Sakakura T (1984) Angew Chem Int Edit 23:518–519CrossRefGoogle Scholar
  206. 206.
    Murahashi SI, Naota T, Nakajima N (1985) Tetrahedron Lett 26:925–928CrossRefGoogle Scholar
  207. 207.
    Murahashi SI, Naota T, Nakajima N (1987) Chem Lett 879–882Google Scholar
  208. 208.
    Kesavan V, Bonnet-Delpon D, Bégué JP, Srikanth A, Chandrasekaran S (2000) Tetrahedron Lett 41:3327–3300CrossRefGoogle Scholar
  209. 209.
    Adair GRA, Williams JMJ (2007) Chem Commun 25:2608–2609CrossRefGoogle Scholar
  210. 210.
    Masutani K, Uchida T, Irie R, Katsuki T (2000) Tetrahedron Lett 41:5119–5123CrossRefGoogle Scholar
  211. 211.
    Ashok M, Prasad AVSS, Reddy PM, Ravinder V (2009) Spectrochim Acta 72A:204–208Google Scholar
  212. 212.
    Xie Y, Zhang Z, Hin S, Li W, Han B (2008) Green Chem 10:278–282CrossRefGoogle Scholar
  213. 213.
    Mizoguchi H, Uchida T, Ishida K, Katsuki T (2009) Tetrahedron Lett 50:3432–3435CrossRefGoogle Scholar
  214. 214.
    Gunanathan C, Shimon LJW, Milstein D (2009) J Am Chem Soc 131:3146–3147CrossRefGoogle Scholar
  215. 215.
    Campestrini S, Carraro M, Franco L, Ciriminna R, Pagliaro M (2008) Tetrahedron Lett 49:419–423CrossRefGoogle Scholar
  216. 216.
    Kogan V, Quintal MM, Neumann R (2005) Org Lett 7:5039–5042CrossRefGoogle Scholar
  217. 217.
    Chatterjeea D, Mitra A, Roy BC (2000) J Mol Catal 161A:17–21CrossRefGoogle Scholar
  218. 218.
    Thangadurai TD, Ihm S-K (2004) Transit Metal Chem 29:189–195CrossRefGoogle Scholar
  219. 219.
    Lee M, Chang S (2000) Tetrahedron Lett 41:7507–7510CrossRefGoogle Scholar
  220. 220.
    Seok WK (1999) Bull Korean Chem Soc 20:395–396Google Scholar
  221. 221.
    Lebeau EL, Meyer TJ (1999) Inorg Chem 38:2174–2181CrossRefGoogle Scholar
  222. 222.
    Catalano VJ, Heck RA, Immoos CE, Öhman A, Hill MG (1998) Inorg Chem 37:2150–2157CrossRefGoogle Scholar
  223. 223.
    Kuznetsova LI, Detusheva LG, Kuznetsova NI, Fedotov MA, Likhobolov VA (1997) J Mol Catal 117A:389–396CrossRefGoogle Scholar
  224. 224.
    Kuznetsova LI, Likholobov VA, Detusheya LG (1993) Kinet Catal (Engl Transl) 34:914–916Google Scholar
  225. 225.
    Mathison CM, Cole-Hamilton DJ (2006) In: Cole-Hamilton DJ, Tooze RP (eds) Catalyst separation, recovery and recycling. Springer, Dordrecht, The Netherlands, p 161Google Scholar
  226. 226.
    Klement I, Lütjens H, Knochel P (1997) Angew Chem Int Edit 36:1454–1456CrossRefGoogle Scholar
  227. 227.
    Fackler NLP, Zhang S, O’Halloran TV (1996) J Am Chem Soc 118:481–482CrossRefGoogle Scholar
  228. 228.
    Inokuchi T, Kanagawa K, Torii S (1995) Tetrahedron Lett 36:3223–3226CrossRefGoogle Scholar
  229. 229.
    Wong KY, Yam VWW, Lee WWS (1992) Electrochim Acta 37:2645–2650CrossRefGoogle Scholar
  230. 230.
    Bäckvall JE, Chowdhury RL, Karlsson U (1991) J Chem Soc Chem Commun 473–475Google Scholar
  231. 231.
    Higuchi T, Ohtake H, Hirobe M (1991) Tetrahedron Lett 32:7433–7438CrossRefGoogle Scholar
  232. 232.
    Che CM, Lai TF, Wong KY (1987) Inorg Chem 26:2289–2299CrossRefGoogle Scholar
  233. 233.
    Wong KY, Che CM, Anson FC (1987) Inorg Chem 26:737–741CrossRefGoogle Scholar
  234. 234.
    Bilgrien C, Davis S, Drago RS (1987) J Am Chem Soc 109:3786–3787CrossRefGoogle Scholar
  235. 235.
    Matsumoto M, Ito S (1981) J Chem Soc Chem Commun 907–908Google Scholar
  236. 236.
    Srivastava S, Srivastava P, Chaudhary L, Kumar A, Singh S (2009) J Indian Chem Soc 86:58–62Google Scholar
  237. 237.
    Ciriminna R, Hesemann P, Moreau JJE, Carraro M, Campestrini S, Pagliaro M (2006) Chem Eur J 12:5220–5224CrossRefGoogle Scholar
  238. 238.
    Cho CS, Kim DY, Shim SC (2005) Bull Korean Chem Soc 26:802–804CrossRefGoogle Scholar
  239. 239.
    Hino T, Wada T, Fujihara T, Tanaka K (2004) Chem Lett 33:1596–1597CrossRefGoogle Scholar
  240. 240.
    Appelbaum L, Heinrichs C, Demtschuk J, Michman M, Oron M, Schäfer HJ, Schumann H (1999) J Organomet Chem 592:240–250CrossRefGoogle Scholar
  241. 241.
    Aït-Mohand S, Lunak S, Muzart J (1997) Chem Ber 130:1655–1658CrossRefGoogle Scholar
  242. 242.
    Tony KJ, Rajaram J, Mahadevan V, Swamy CS (1997) React Kinet Catal Lett 60:145–155CrossRefGoogle Scholar
  243. 243.
    Boelrijk AM, Dorst HT, Reedijk J (1996) Rec Trav Chim 115:536–541CrossRefGoogle Scholar
  244. 244.
    Boelrijk AEM, Reedijk J (1994) Rec Trav Chim 113:411–412Google Scholar
  245. 245.
    Karlsson U, Wang GZ, Bäckvall JE (1994) J Org Chem 59:1196–1198CrossRefGoogle Scholar
  246. 246.
    Murahashi SI, Naota T, Hirai N (1993) J Org Chem 58:7318–7319CrossRefGoogle Scholar
  247. 247.
    Li CK, Che CM, Tong WF, Tang WT, Wong KY, Lai TF (1992) J Chem Soc Dalton Trans 13:2109–2116CrossRefGoogle Scholar
  248. 248.
    Lee DG, Wang Z, Chandler WD (1992) J Org Chem 57:3276–3277CrossRefGoogle Scholar
  249. 249.
    El-Hendawy AM, El-Kourashy AE, Shanab MM (1992) Polyhedron 11:523–530CrossRefGoogle Scholar
  250. 250.
    Wang GZ, Bäckvall JE (1992) J Chem Soc Chem Commun 337–339Google Scholar
  251. 251.
    El-Hendawy AM (1992) Transit Metal Chem 17:250–255CrossRefGoogle Scholar
  252. 252.
    Ohtake H, Higuchi T, Hirobe M (1992) J Am Chem Soc 114:10660–10662CrossRefGoogle Scholar
  253. 253.
    El-Hendawy EM (1991) Polyhedron 10:2511–2518CrossRefGoogle Scholar
  254. 254.
    Lee DG, Congson LN (1990) Can J Chem 68:1774–1779CrossRefGoogle Scholar
  255. 255.
    Taqui Khan MM, Shukla RS, Rao AP (1989) Inorg Chem 28:452–458CrossRefGoogle Scholar
  256. 256.
    Bressan M, Morvillo A (1989) J Chem Soc Chem Commun 421–423Google Scholar
  257. 257.
    Taqui Khan MM, Shukla RS (1989) J Mol Catal 51:171–180CrossRefGoogle Scholar
  258. 258.
    Lee DG, Spitzer UA, Cleland J, Olson ME (1976) Can J Chem 54:2124–2126CrossRefGoogle Scholar
  259. 259.
    Lee DG, van der Engh M (1972) Can J Chem 50:2000–2009CrossRefGoogle Scholar
  260. 260.
    Lee DG, Congson LN, Spitzer UA, Olson ME (1984) Can J Chem 62:1835–1839CrossRefGoogle Scholar
  261. 261.
    Thompson MS, De Giovani WF, Moyer BA, Meyer TJ (1984) J Org Chem 49:4972–4977CrossRefGoogle Scholar
  262. 262.
    Becker P, Beattie JK (1982) Aust J Chem 35:1245–1249CrossRefGoogle Scholar
  263. 263.
    Thompson MS, Meyer TJ (1982) J Am Chem Soc 104:4106–4115CrossRefGoogle Scholar
  264. 264.
    Sathya N, Manimaran A, Raja G, Muthusamy P, Deivasigamani K, Jayabalakrishnan C (2009) Transit Metal Chem 34:7–13CrossRefGoogle Scholar
  265. 265.
    Sathya N, Muthusamy P, Padmapriya N, Raja G, Deivasigamani K, Jayabalakrishnan C (2009) J Coord Chem 62:3532–3543CrossRefGoogle Scholar
  266. 266.
    Muthukumar M, Viswanathamurti P (2009) Appl Organomet Chem 23:78–85CrossRefGoogle Scholar
  267. 267.
    Muthukumar M, Viswanathamurti P (2009) Spectrochim Acta 74A:454–462Google Scholar
  268. 268.
    Kuiper JL, Shapley PA (2007) J Organomet Chem 692:1653–1660CrossRefGoogle Scholar
  269. 269.
    Hamamoto H, Kudoh M, Takahashi H, Natsugari H, Ikegami S (2007) Chem Lett 36:632–633CrossRefGoogle Scholar
  270. 270.
    Komiya N, Nakae T, Sato H, Naota T (2006) Chem Commun 4829–4831Google Scholar
  271. 271.
    Kobayashi S, Miyamura H, Akiyama R, Ishida T (2005) J Am Chem Soc 127:9251–9254CrossRefGoogle Scholar
  272. 272.
    Gauthier S, Scopelliti R, Severin K (2004) Organometallics 23:3769–3771CrossRefGoogle Scholar
  273. 273.
    Wolfson A, Wuyts S, de Vos DE, Vankelcom IFJ, Jacobs PA (2002) Tetrahedron Lett 43:8107–8110CrossRefGoogle Scholar
  274. 274.
    El-Hendawy AM, Alqaradawi SY, Al-Madfa HA (2000) Transit Metal Chem 25:572–578CrossRefGoogle Scholar
  275. 275.
    Bhowon MG, Wah HLK, Narain N (1999) Polyhedron 18:341–345CrossRefGoogle Scholar
  276. 276.
    Fung WH, Yu WY, Che CM (1998) J Org Chem 63:2873–2877CrossRefGoogle Scholar
  277. 277.
    Wang Z, Chandler WD, Lee DG (1998) Can J Chem 76:919–928CrossRefGoogle Scholar
  278. 278.
    Navarro M, De Giovani WF, Romero JS (1998) J Mol Catal 135A:249–256CrossRefGoogle Scholar
  279. 279.
    El-Hendawy AM, Al-Kubaisi AH, Al-Madfa HA (1997) Polyhedron 16:3039–3045CrossRefGoogle Scholar
  280. 280.
    Boelrijk AEM, Neenan TX, Reedijk J (1997) J Chem Soc Dalton Trans 4561–4570Google Scholar
  281. 281.
    Tony KI, Mahadven V, Rajaram I, Swamy CS (1996) Int J Chem Kinet 28:657–663Google Scholar
  282. 282.
    Neyhart GA, Cheng CC, Thorp HH (1995) J Am Chem Soc 117:1463–1471CrossRefGoogle Scholar
  283. 283.
    Bailey AJ, Griffith WP, Savage PD (1995) J Chem Soc Dalton Trans 3537–3542Google Scholar
  284. 284.
    Nam JH, Kwon JH, Yang SB (1994) Bull Korean Chem Soc 15:692–694Google Scholar
  285. 285.
    El-Hendawy AM, Alkubaisi AH, El-Kourashy AE, Shanab MM (1993) Polyhedron 12:2343–2350CrossRefGoogle Scholar
  286. 286.
    Griffith WP, Jolliffe JM (1992) J Chem Soc Dalton Trans 3483–3488Google Scholar
  287. 287.
    Griffith WP, Jolliffe JM (1991) In: Simándi LI (ed) Dioxygen activation and homogeneous catalytic oxidation. Elsevier Science Publishers B. V, Amsterdam, pp 395–400CrossRefGoogle Scholar
  288. 288.
    Che CI, Tang WT, Lee WO, Wong KY, Lau TC (1992) J Chem Soc Dalton Trans 1551–1556Google Scholar
  289. 289.
    Muller JG, Acquaye JH, Takeuchi KJ (1992) Inorg Chem 31:4552–4557CrossRefGoogle Scholar
  290. 290.
    Che CM, Ho C, Lau TC (1991) J Chem Soc Dalton Trans 1259–1263Google Scholar
  291. 291.
    Che CM, Yam VWW, Mak TCW (1990) J Am Chem Soc 112:2284–2291CrossRefGoogle Scholar
  292. 292.
    Dengel AC, El-Hendawy AM, Griffith WP, O’Mahoney CA, Williams DJ (1990) J Chem Soc Dalton Trans 737–742Google Scholar
  293. 293.
    El-Hendawy AM, Griffith WP, Taha FI, Moussa MN (1989) J Chem Soc Dalton Trans 901–906Google Scholar
  294. 294.
    El-Hendawy AM, Griffith WP, Piggott B, Williams DJ (1988) J Chem Soc Dalton Trans 1983–1988Google Scholar
  295. 295.
    Dengel AC, El-Hendawy AM, Griffith WP, Mostafa SI, Williams DJ (1992) J Chem Soc Dalton Trans 3489–3495Google Scholar
  296. 296.
    Griffith WP, Jolliffe JM, Ley SV, Williams DJ (1990) J Chem Soc Chem Commun 1219–1221Google Scholar
  297. 297.
    Che CM, Leung WH, Li CK, Poon CK (1991) J Chem Soc Dalton Trans 379–384Google Scholar
  298. 298.
    El-Hendawy AM (1991) Polyhedron 10:2137–2143CrossRefGoogle Scholar
  299. 299.
    Caroling G, Rajaram J, Kuiriacose JC (1990) J Mol Catal 58:235–243CrossRefGoogle Scholar
  300. 300.
    Taqui Khan MM, Shukla RS (1989) J Mol Catal 54:45–55CrossRefGoogle Scholar
  301. 301.
    Barak G, Dakka J, Sasson Y (1988) J Org Chem 53:3553–3555CrossRefGoogle Scholar
  302. 302.
    Roecker L, Meyer TJ (1987) J Am Chem Soc 109:746–754CrossRefGoogle Scholar
  303. 303.
    Gagné RR, Marks DN (1984) Inorg Chem 23:65–74CrossRefGoogle Scholar
  304. 304.
    Matsumoto M, Ito S (1984) Synth Commun 14:697–700CrossRefGoogle Scholar
  305. 305.
    Kanemoto S, Oshima K, Matsubara S, Takai K, Nozaki H (1983) Tetrahedron Lett 24:2185–2188CrossRefGoogle Scholar
  306. 306.
    Müller P, Godoy J (1981) Tetrahedron Lett 22:2361–2364CrossRefGoogle Scholar
  307. 307.
    Moyer BA, Thompson MS, Meyer TJ (1980) J Am Chem Soc 102:2310–2312CrossRefGoogle Scholar
  308. 308.
    Morris PE, Kiely DE (1987) J Org Chem 52:1149–1152CrossRefGoogle Scholar
  309. 309.
    Regen SL, Whitesides GM (1972) J Org Chem 37:1832–1833CrossRefGoogle Scholar
  310. 310.
    Beynon PJ, Collins PM, Overend WG (1964) Proc Chem Soc 242–243Google Scholar
  311. 311.
    Butterworth RF, Hanessian S (1971) Synthesis 70–83Google Scholar
  312. 312.
    Beynon PJ, Collins PM, Gardiner D, Overend WG (1968) Carbohydr Res 6:431–425CrossRefGoogle Scholar
  313. 313.
    Beynon PJ, Collins PM, Doganges PT, Overend WG (1966) J Chem Soc (C) 1131–1136Google Scholar
  314. 314.
    Horton D, Tindall CG (1970) Carbohydr Res 15:215–232CrossRefGoogle Scholar
  315. 315.
    Collins PM, Hurford JR, Overend WG (1975) J Chem Soc Perkin Trans 1:2163–2177CrossRefGoogle Scholar
  316. 316.
    Nutt RF, Dickinson MJ, Holly FW, Walton E (1968) J Org Chem 33:1789–1795CrossRefGoogle Scholar
  317. 317.
    Collins PM, Doganges PT, Kolarikol A, Overend WG (1969) Carbohydr Res 11:199–206CrossRefGoogle Scholar
  318. 318.
    Albano EL, Horton D (1969) Carbohydr Res 11:485–495CrossRefGoogle Scholar
  319. 319.
    Brimacombe JS, Hunedy F, Al-Radhi AK (1969) Carbohydr Res 11:331–340CrossRefGoogle Scholar
  320. 320.
    Horton D, Just EK (1969) Carbohydr Res 9:129–137CrossRefGoogle Scholar
  321. 321.
    Horton D, Jewell JS (1967) Carbohydr Res 5:149–160CrossRefGoogle Scholar
  322. 322.
    Nahar S, Overend WG, Williams NR (1967) Chem Ind (London) 2114–2115Google Scholar
  323. 323.
    Howarth GB, Jones JKN (1967) Can J Chem 45:2253–2256CrossRefGoogle Scholar
  324. 324.
    Horton D, Jewell JS (1966) Carbohydr Res 2:251–260CrossRefGoogle Scholar
  325. 325.
    Nutt RF, Arison B, Holly FW, Walton E (1965) J Am Chem Soc 87:3273CrossRefGoogle Scholar
  326. 326.
    Rosenthal A, Sprinzl M, Baker DA (1970) Tetrahedron Lett 4233–4235Google Scholar
  327. 327.
    Slessor KN, Tracey AS (1969) Can J Chem 47:3989–3995CrossRefGoogle Scholar
  328. 328.
    Gonsalvi L, Arends IWCE, Sheldon RA (2002) Org Lett 4:1659–1661CrossRefGoogle Scholar
  329. 329.
    Baker DC, Horton D, Tindall CG (1976) Methods Carbohydr Chem 7:3–6Google Scholar
  330. 330.
    Lawton BT, Szarek WA, Jones JKN (1969) Carbohydr Res 10:456–458CrossRefGoogle Scholar
  331. 331.
    Howarth GB, Szarek WA, Jones JKN (1968) Carbohydr Res 7:284–290CrossRefGoogle Scholar
  332. 332.
    Baggett N, Stribblehill P (1981) Carbohydr Res 96:41–58CrossRefGoogle Scholar
  333. 333.
    Stevens CL, Bryant CP (1975) Methods Carbohydr Chem 6:337–341Google Scholar
  334. 334.
    Singh AK, Varma RS (1992) Tetrahedron Lett 33:2307–2310CrossRefGoogle Scholar
  335. 335.
    Varma RS, Hogan ME (1992) Tetrahedron Lett 33:7719–7720CrossRefGoogle Scholar
  336. 336.
    Smejkal J, Kalvoda L (1973) Coll Czech Chem Commun 38:1981–1984CrossRefGoogle Scholar
  337. 337.
    Boelrijk AEM, Reedijk J (1994) J Mol Catal 89:63–76CrossRefGoogle Scholar
  338. 338.
    Cronin L, Murphy PV (2005) Org Lett 7:2691–2693CrossRefGoogle Scholar
  339. 339.
    Endo T, Zemlička J (1979) J Org Chem 44:3652–3656CrossRefGoogle Scholar
  340. 340.
    Tipson RS, Brady RF, West BF (1971) Carbohydr Res 16:383–393CrossRefGoogle Scholar
  341. 341.
    Dolphin D, James BR, Leung TW (1983) Inorg Chim Acta 79:25–27CrossRefGoogle Scholar
  342. 342.
    Flaherty B, Overend WG, Williams NR (1966) J Chem Soc (C) 398–403Google Scholar
  343. 343.
    Désiré E, Dransfield PJ, Shipman MS (2001) Synlett 1329–1331Google Scholar
  344. 344.
    Matsuura D, Mitsui T, Sengoku T, Takahashi M, Yoda H (2008) Tetrahedron 64:11686–11696CrossRefGoogle Scholar
  345. 345.
    Shing TKM, Cheng HM (2007) J Org Chem 72:6610–6613CrossRefGoogle Scholar
  346. 346.
    Paquette L, Tian Z, Seekamp CK, Wang T (2005) Helv Chim Acta 88:1185–1198CrossRefGoogle Scholar
  347. 347.
    Desjardins M, Brammer LE, Hudlický T (1997) Carbohydr Res 304:39–42CrossRefGoogle Scholar
  348. 348.
    Daneault C, Kokta BV, Cheradame H (1983) J Wood Chem Tech 3:459–472CrossRefGoogle Scholar
  349. 349.
    Shigemasa Y, Sashiwa H, Nakamura K, Takeuchi Y, Saimoto H (1991) Polym J 23:1279–1281CrossRefGoogle Scholar
  350. 350.
    Jain SL, Sharma VB, Sain B (2005) Synth Commun 35:465–469CrossRefGoogle Scholar
  351. 351.
    Acosta CK, Rao PN, Kim HK (1993) Steroids 58:205–208CrossRefGoogle Scholar
  352. 352.
    Carter R, Hodgetts K, McKenna J, Magnus P, Wren S (2000) Tetrahedron 56:4367–4382CrossRefGoogle Scholar
  353. 353.
    Mehta G, Karra SR (1991) Tetrahedron Lett 32:3215–3216CrossRefGoogle Scholar
  354. 354.
    Shih TL, Mrozik H, Holmes MA, Arison BH, Doss GA, Waksmunski F, Fisher MH (1992) Tetrahedron Lett 33:1709–1712CrossRefGoogle Scholar
  355. 355.
    Hirota H, Yokoyama A, Miyaji K, Nakamura T, Takahashi T (1987) Tetrahedron Lett 25:435–438CrossRefGoogle Scholar
  356. 356.
    Hollinshead DM, Howell SC, Ley SV, Mahon M, Worthington PA (1983) J Chem Soc Perkin Trans 1:1579–1589CrossRefGoogle Scholar
  357. 357.
    Mehta G, Karra SR (1991) J Chem Soc Chem Commun 1367–1368Google Scholar
  358. 358.
    Larrosa I, Da Silva MI, Gómez PM, Hannen P, Ko E, Lenger SR, Linke SR, White AJP, Wilton D, Barrett AGM (2006) J Am Chem Soc 128:14042–14043CrossRefGoogle Scholar
  359. 359.
    Merten J, Hennig A, Schwab P, Fröhlich R, Tokalov SV, Gutzeit HO, Metz P (2006) Eur J Chem 1144–1161Google Scholar
  360. 360.
    Kim J-Y, Wang P, Navarro-Villalobos M, Rohde VD, Derryberry J, Gin DY (2006) J Am Chem Soc 128:11906–11915CrossRefGoogle Scholar
  361. 361.
    Göksel H, Stark CBW (2006) Org Lett 8:3433–3436CrossRefGoogle Scholar
  362. 362.
    Miyaoka H, Hara Y, Shinohara I, Kurokawa T, Yamada Y (2005) Tetrahedron Lett 46:7945–7949CrossRefGoogle Scholar
  363. 363.
    Shimizu H, Onitsuka S, Egami H, Katsuki T (2005) J Am Chem Soc 127:5396–5413CrossRefGoogle Scholar
  364. 364.
    Trost BM, Rhee YH (2004) Org Lett 6:4311–4313CrossRefGoogle Scholar
  365. 365.
    Trost BM, Rhee YH (2002) J Am Chem Soc 124:2528–2533CrossRefGoogle Scholar
  366. 366.
    MacCoss RN, Balskus EP, Ley SV (2003) Tetrahedron Lett 44:7779–7781CrossRefGoogle Scholar
  367. 367.
    Markó IE, Gautier A, Tsukazaki M, Llobet A, Plantalech-Mir E, Urch CJ, Brown SM (1999) Angew Chem Int Edit 38:1960–1961CrossRefGoogle Scholar
  368. 368.
    Owston NA, Nixon TD, Parker AJ, Whittlesey MK, Williams JMJ (2009) Synthesis 1578–1581Google Scholar
  369. 369.
    Owston NA, Parker AJ, Williams JMJ (2008) Chem Commun 624–625Google Scholar
  370. 370.
    Watanabe T, Nishiyama S, Yamamura S, Kato K, Nagai M, Takita T (1991) Tetrahedron Lett 32:2399–2400CrossRefGoogle Scholar
  371. 371.
    Maki BE, Scheidt KA (2009) Org Lett 11:1651–1654CrossRefGoogle Scholar
  372. 372.
    Hall MI, Pridmore SJ, Williams SMJ (2008) Adv Synth Catal 350:1975–1978Google Scholar

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© Springer Netherlands 2009

Authors and Affiliations

  1. 1.Department of ChemistryImperial CollegeLondonUnited Kingdom

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