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Chiral Phosphorus Ligands with Interesting Properties and Practical Applications

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Asymmetric Catalysis from a Chinese Perspective

Part of the book series: Topics in Organometallic Chemistry ((TOPORGAN,volume 36))

Abstract

Asymmetric transformations using a catalytic approach remain significantly important in organic synthesis, especially in the preparation of pharmaceutically interesting molecules. Indeed, chiral phosphorus ligands play an important role in this area. In this chapter, the recent development and advancement of chiral phosphines, phosphites, phosphoramides, etc. are reviewed. The potentially practical organic transformations are also described.

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References

  1. Ojima I (2000) Wiley-VCH, Weinheim

    Google Scholar 

  2. Jacobsen EN, Pfaltz A, Yamamoto H (1999) Springer, Berlin

    Google Scholar 

  3. Cornils B, Herrmann WA (2002) Wiley-VCH, Weinheim

    Google Scholar 

  4. Benincori T, Rizzo S, Sannicolò F (2002) J Heterocycl Chem 39:471–485

    CAS  Google Scholar 

  5. Kurtev K, Ribola D, Jones RA, Cole-Hamilton DJ, Wilkinson G (1980) J Chem Soc Dalton Trans Inorg Chem 1:55–58

    Google Scholar 

  6. Hu W, Pai CC, Chen CC, Xue G, Chan ASC (1998) Tetrahedron: Asymmetry 9:3241–3246

    CAS  Google Scholar 

  7. Hu W, Chen CC, Xue G, Chan ASC (1998) Tetrahedron: Asymmetry 9:4183–4192

    CAS  Google Scholar 

  8. Pai CC, Lin CW, Lin CC, Chen CC, Chan ASC, Wong WT (2000) J Am Chem Soc 122:11513–11514

    CAS  Google Scholar 

  9. Wu J, Chen H, Zhou ZY, Yeung CH, Chan ASC (2001) Synlett:1050–1054

    Google Scholar 

  10. Wu J, Chen H, Kwok WH, Lam KH, Zhou ZY, Yeung CH, Chan ASC (2002) Tetrahedron Lett 43:1539–1543

    CAS  Google Scholar 

  11. Wu J, Au-Yeung TTL, Kwok WH, Ji JX, Zhou Z, Yeung CH, Chan ASC (2005) Adv Synth Catal 347:507–511

    CAS  Google Scholar 

  12. Pai CC, Li YM, Zhou ZY, Chan ASC (2002) Tetrahedron Lett 43:2789–2792

    CAS  Google Scholar 

  13. Duprat de Paule S, Jeulin S, Ratovelomanana-Vidal V, Genêt JP, Champion N, Dellis P (2003) Tetrahedron Lett 44:823–826

    CAS  Google Scholar 

  14. Tuyet TMT, Harada T, Hashimoto K, Hatsuda M, Oku A (2000) J Org Chem 65:1335–1343

    CAS  Google Scholar 

  15. Bringmann G, Menche D (2001) Acc Chem Res 34:615–624

    CAS  Google Scholar 

  16. Yin J, Buchwald SL (2000) J Am Chem Soc 122:12051–12052

    CAS  Google Scholar 

  17. Hayashi T, Hayashizaki K, Kiyoi T, Ito Y (1988) J Am Chem Soc 110:8153–8156

    CAS  Google Scholar 

  18. Barhate NB, Chen CT (2002) Org Lett 4:2529–2532

    CAS  Google Scholar 

  19. Nicolaou KC, Li H, Boddy CNC, Ramanjulu JM, Yue TJ, Bräse S, Rübsam F (1999) Chem Eur J 5:2584–2601

    CAS  Google Scholar 

  20. Cammidge AN, Crépy KVL (2000) Chem Commun 18:1723–1724

    Google Scholar 

  21. Kano T, Ohyabu Y, Saito S, Yamamoto H (2002) J Am Chem Soc 124:5365–5373

    CAS  Google Scholar 

  22. Itoh T, Chika Ji (1995) J Org Chem 60:4968–4969

    CAS  Google Scholar 

  23. Lipshutz BH, Kayser F, Liu ZP (1994) Angew Chem Int Ed Engl 33:1842–1844

    Google Scholar 

  24. Lipshutz BH, James B, Vance S, Carrico I (1997) Tetrahedron Lett 38:753–756

    CAS  Google Scholar 

  25. Lin GQ, Zhong M (1997) Tetrahedron Lett 38:1087–1090

    CAS  Google Scholar 

  26. Nelson TD, Meyers AI (1994) Tetrahedron Lett 35:3259–3262

    CAS  Google Scholar 

  27. Nelson TD, Meyers AI (1994) J Org Chem 59:2655–2658

    CAS  Google Scholar 

  28. Nelson TD, Meyers AI (1993) Tetrahedron Lett 34:3061–3062

    CAS  Google Scholar 

  29. Rawai VH, Florjancic AS, Singh SP (1994) Tetrahedron Lett 35:8985–8988

    Google Scholar 

  30. Ku YY, Grieme T, Raje P, Sharma P, King SA, Morton HE (2002) J Am Chem Soc 124:4282–4286

    CAS  Google Scholar 

  31. Michaud G, Bulliard M, Ricard L, Genêt JP, Marinetti A (2002) Chem Eur J 8:3327–3330

    CAS  Google Scholar 

  32. Miyano S, Fukushima H, Handa S, Ito H, Hashimoto H (1988) Bull Chem Soc Jpn 61:3249–3254

    CAS  Google Scholar 

  33. Nelson SG, Hilfiker MA (1999) Org Lett 1:1379–1382

    CAS  Google Scholar 

  34. Spring DR, Krishnan S, Blackwell HE, Schreiber S (2002) J Am Chem Soc 124:1354–1363

    CAS  Google Scholar 

  35. Kamikawa K, Watanabe T, Uemura M (1996) J Org Chem 61:1375–1384

    CAS  Google Scholar 

  36. Vorogushin AV, Wulff WD, Hansen HJ (2002) J Am Chem Soc 124:6512–6513

    CAS  Google Scholar 

  37. Qiu L, Qi J, Pai CC, Chan S, Zhou Z, Choi MCK, Chan ASC (2002) Org Lett 4:4599–4602

    CAS  Google Scholar 

  38. Qiu L, Wu J, Chan S, Au-Yeung TTL, Ji JX, Guo R, Pai CC, Zhou Z, Li X, Fan QH, Chan ASC (2004) Proc Natl Acad Sci USA 101:5815–5820

    CAS  Google Scholar 

  39. Qiu L, Kwong FY, Wu J, Lam WH, Chan S, Yu WY, Li YM, Guo R, Zhou Z, Chan ASC (2006) J Am Chem Soc 128:5955–5965

    CAS  Google Scholar 

  40. Wu J, Chan ASC (2006) Acc Chem Res 39:711–720

    CAS  Google Scholar 

  41. Lam WS, Kok SHL, Au-Yeung TTL, Wu J, Cheung HY, Lam FL, Yeung CH, Chan ASC (2006) Adv Synth Catal 348:370–374

    CAS  Google Scholar 

  42. Lam FL, Au-Yeung TTL, Cheung HY, Kok SHL, Lam WS, Wong KY, Chan ASC (2006) Tetrahedron: Asymmetry 17:497–499

    CAS  Google Scholar 

  43. Okoroafor MO, Ward DL, Brubaker CH (1988) Organometallics 7:1504–1511

    CAS  Google Scholar 

  44. Fernández I, Valdivia V, Gori B, Alcudia F, Álvarez E, Khiar N (2005) Org Lett 7:1307–1310

    Google Scholar 

  45. Cheung HY, Yu WY, Lam FL, Au-Yeung TTL, Zhou ZY, Chan TH, Chan ASC (2007) Org Lett 9:4295–4298

    CAS  Google Scholar 

  46. Chan ASC, Pai CC (1999) US 5886182

    Google Scholar 

  47. Lin GQ, Li YM, Chan ASC (2001) Wiley, New York

    Google Scholar 

  48. Tang W, Zhang X (2003) Chem Rev 103:3029–3070

    CAS  Google Scholar 

  49. Shimizu H, Nagasaki I, Saito T (2005) Tetrahedron 61:5405–5432

    CAS  Google Scholar 

  50. Kitamura M, Tsukamoto M, Bessho Y, Yoshimura M, Kobs U, Widhalm M, Noyori R (2002) J Am Chem Soc 124:6649–6667, and references therein

    CAS  Google Scholar 

  51. Wu J, Pai CC, Kwok WH, Guo RW, Au-Yeung TTL, Yeung CH, Chan ASC (2003) Tetrahedron: Asymmetry 14:987–992

    CAS  Google Scholar 

  52. Juaristi E (1997) Wiley-VCH, New York

    Google Scholar 

  53. Lubell WD, Kitamura M, Noyori R (1991) Tetrahedron: Asymmetry 2:543–554

    CAS  Google Scholar 

  54. Wu J, Chen X, Guo R, Yeung CH, Chan ASC (2003) J Org Chem 68:2490–2493

    CAS  Google Scholar 

  55. Duprat de Paule S, Jeulin S, Ratovelomanana-Vidal V, Genêt JP, Champion N, Dellis P (2003) Eur J Org Chem 10:1931–1941

    Google Scholar 

  56. Benincori T, Cesarotti E, Piccolo O, Sannicolo F (2000) J Org Chem 65:2043–2047

    CAS  Google Scholar 

  57. Saito T, Yokozawa T, Ishizaki T, Moroi T, Sayo N, Miura T, Kumobayashi H (2001) Adv Synth Catal 343:264–267

    CAS  Google Scholar 

  58. Chiba T, Miyashita A, Nohira H, Takaya H (1993) Tetrahedron Lett 34:2351–2354

    CAS  Google Scholar 

  59. Mashima K, Kusano KH, Sato N, Matsumura YI, Nozaki K, Kumobayashi H, Sayo N, Hori Y, Ishizaki T, Akutagawa S, Takaya H (1994) J Org Chem 59:3064–3076

    CAS  Google Scholar 

  60. Hapiot F, Agbossou F, Mortreux A (1995) Tetrahedron: Asymmetry 6:11–14

    CAS  Google Scholar 

  61. Carpentier JF, Mortreux A (1997) Tetrahedron: Asymmetry 8:1083–1099

    CAS  Google Scholar 

  62. Burk MJ, Pizzano A, Martin JA (2000) Organometallics 19:250–260

    CAS  Google Scholar 

  63. Boaz NW, Debenham SD, Mackenzie EB, Large SE (2002) Org Lett 4:2421–2424

    CAS  Google Scholar 

  64. Boaz NW, Mackenzie EB, Debenham SD, Large SE, Ponasik JA (2005) J Org Chem 70:1872–1880

    CAS  Google Scholar 

  65. Ager DJ, Laneman SA (1997) Tetrahedron: Asymmetry 8:3327–3355

    CAS  Google Scholar 

  66. Noyori R, Ohkuma T (2001) Angew Chem Int Ed 40:40–73

    CAS  Google Scholar 

  67. Noyori R, Ohkuma T, Kitamura M, Takaya H, Sayo N, Kumobayashi H, Akutagawa S (1987) J Am Chem Soc 109:5856–5858

    CAS  Google Scholar 

  68. Kitamura M, Ohkuma T, Takaya H, Noyori R (1988) Tetrahedron Lett 29:1555–1556

    CAS  Google Scholar 

  69. Chan ASC, Chen J (2006) CN 1727328 A

    Google Scholar 

  70. Pu L, Yu HB (2001) Chem Rev 101:757–824

    CAS  Google Scholar 

  71. Doucet H, Ohkuma T, Murata K, Yokozawa T, Kozawa M, Katayama E, England AF, Ikariya T, Noyori R (1998) Angew Chem Int Ed Engl 37:1703–1707

    CAS  Google Scholar 

  72. Gokel G, Marquarding D, Ugi I (1972) J Org Chem 37:3052–3058

    CAS  Google Scholar 

  73. Marquarding D, Klusacek H, Gokel G, Hoffmann P, Ugi I (1970) J Am Chem Soc 92:5389–5393

    CAS  Google Scholar 

  74. Ohta T, Miyake T, Seido N, Kumobayashi H, Takaya H (1995) J Org Chem 60:357–363

    CAS  Google Scholar 

  75. Wu S, Wang W, Tang W, Lin M, Zhang X (2002) Org Lett 4:4495–4497

    CAS  Google Scholar 

  76. Nishiyama H, Itoh K (2000) Wiley-VCH, New York

    Google Scholar 

  77. Carpentier JF, Bette V (2002) Curr Org Chem 6:913–936

    CAS  Google Scholar 

  78. Appella DH, Moritani Y, Shintani R, Ferreira EM, Buchwald SL (1999) J Am Chem Soc 121:9473–9474

    CAS  Google Scholar 

  79. Hughes G, Kimura M, Buchwald SL (2003) J Am Chem Soc 125:11253–11258

    CAS  Google Scholar 

  80. Lipshutz BH, Noson K, Chrisman W (2001) J Am Chem Soc 123:12917–12918

    CAS  Google Scholar 

  81. Lipshutz BH, Noson K, Chrisman W, Lower A (2003) J Am Chem Soc 125:8779–8789

    CAS  Google Scholar 

  82. Lipshutz BH, Lower A, Noson K (2002) Org Lett 4:4045–4048

    CAS  Google Scholar 

  83. Lipshutz BH, Frieman BA (2005) Angew Chem Int Ed 44:6345–6348

    CAS  Google Scholar 

  84. Rainka MP, Aye Y, Buchwald SL (2004) Proc Natl Acad Sci USA 101:5821–5823

    CAS  Google Scholar 

  85. Sirol S, Courmarcel J, Mostefai N, Riant O (2001) Org Lett 3:4111–4113

    CAS  Google Scholar 

  86. Wu J, Ji JX, Chan ASC (2005) Proc Natl Acad Sci USA 102:3570–3575

    CAS  Google Scholar 

  87. Lawrence NJ, Drew MD, Bushell SM (1999) J Chem Soc Perkin Trans 1:3381–3391

    Google Scholar 

  88. Brunner H, Kürzinger A (1988) J Organometal Chem 346:413–424

    CAS  Google Scholar 

  89. Uskoković MR, Lewis RL, Partridge JJ, Despreaux CW, Pruess DL (1979) J Am Chem Soc 101:6742–6744

    Google Scholar 

  90. Deeter J, Frazier J, Staten G, Staszak M, Weigel L (1990) Tetrahedron Lett 31:7101–7104

    CAS  Google Scholar 

  91. Lukevics É, Ioveĭ I, Rubina K, Popelis Y, Gaukhman A (1996) Chem Heterocycl Compd 32:294–307

    Google Scholar 

  92. Zhang XC, Wu Y, Yu F, Wu FF, Wu J, Chan ASC (2009) Chem Eur J 15:5888–5891

    CAS  Google Scholar 

  93. Kumar A, Ner DH, Dike SY (1991) Tetrahedron Lett 32:1901–1904

    CAS  Google Scholar 

  94. Trost BM, Fleming I (1991) Pergamon, Oxford

    Google Scholar 

  95. Barton D HR, Nakanishi K, Meth-Cohn O (1999) Elsevier, Oxford

    Google Scholar 

  96. Katritzky AR, Rachwal S, Rachwal B (1996) Tetrahedron 52:15031–15070, and references therein

    CAS  Google Scholar 

  97. Wang WB, Lu SM, Yang PY, Han XM, Zhou YG (2003) J Am Chem Soc 125:10536–10537

    CAS  Google Scholar 

  98. Yang PY, Zhou YG (2004) Tetrahedron: Asymmetry 15:1145–1149

    CAS  Google Scholar 

  99. Lu SM, Han XM, Zhou YG (2004) Adv Synth Catal 346:909–912

    CAS  Google Scholar 

  100. Xu L, Lam KH, Ji J, Wu J, Fan QH, Lo WH, Chan ASC (2005) Chem Commun:1390–1392

    Google Scholar 

  101. Jacobsen EJ, Stelzer LS, Belonga KL, Carter DB, Im WB, Sethy VH, Tang AH, VonVoigtlander PJD (1996) J Med Chem 39:3820–3836

    CAS  Google Scholar 

  102. Sikorski JA (2006) J Med Chem 49:1–22

    CAS  Google Scholar 

  103. Ohtake Y, Naito A, Hasegawa H, Kawano K, Morizono D, Tangiguchi M, Tanaka Y, Matsukawa H, Naito K, Oguma T, Ezure Y, Tsuriya Y (1999) Bioorg Med Chem 7:1247–1254

    CAS  Google Scholar 

  104. Torisu K, Kobayashi K, Iwahashi M, Nakai Y, Onoda T, Nagase T, Sugimoto I, Okada Y, Matsumoto R, Nanbu F, Ohuchida S, Nakai H, Toda M (2004) Bioorg Med Chem 12:5361–5378

    CAS  Google Scholar 

  105. Eary CT, Jones ZS, Groneberg RD, Burgess LE, Mareska DA, Drew MD, Blake JF, Laird ER, Balachari D, Sullivan MO, Allen A, Marsh V (2007) Bioorg Med Chem Lett 17:2608–2613

    CAS  Google Scholar 

  106. Jones Z, Groneberg R, Drew M, Eary CT (2005) US 20050282812

    Google Scholar 

  107. Murata S, Sugimoto T, Matsuura S (1987) Heterocycles 26:763–766

    CAS  Google Scholar 

  108. Bianchini C, Barbaro P, Scapacci G, Farnetti E, Graziani M (1998) Organometallics 17:3308–3310

    CAS  Google Scholar 

  109. Bianchini C, Barbaro P, Scapacci G (2001) J Organomet Chem 621:26–33

    CAS  Google Scholar 

  110. Cobley CJ, Henschke JP (2003) Adv Synth Catal 345:195–201

    CAS  Google Scholar 

  111. Henschke JP, Burk MJ, Malan CG, Herzberg D, Peterson JA, Wildsmith AJ, Cobley CJ, Casy G (2003) Adv Synth Catal 345:300–307

    CAS  Google Scholar 

  112. Tang W, Xu L, Fan QH, Wang J, Fan B, Zhou Z, Lam KH, Chan ASC (2009) Angew Chem Int Ed 48:9135–9138

    CAS  Google Scholar 

  113. Nefkens SCA, Sperrle M, Consiglio G (1993) Angew Chem Int Ed Engl 2:1719–1720

    Google Scholar 

  114. Wang L, Kwok WH, Wu J, Guo R, Au-Yeung TT, Zhou Z, Chan ASC, Chan KS (2003) J Mol Catal A 196:171–178

    CAS  Google Scholar 

  115. Corey EJ, Guzman-Perez A (1998) Angew Chem Int Ed 37:388–401

    Google Scholar 

  116. Christoffers J, Mann A (2001) Angew Chem Int Ed 40:4591–4597

    CAS  Google Scholar 

  117. Denissova I, Barriault L (2003) Tetrahedron 59:10105–10146

    CAS  Google Scholar 

  118. Douglas CJ, Overman LE (2004) Proc Natl Acad Sci USA 101:5363–5367

    CAS  Google Scholar 

  119. Wu J, Mampreian DM, Hoveyda AH (2005) J Am Chem Soc 127:4584–4585

    CAS  Google Scholar 

  120. Hird AW, Hoveyda AH (2005) J Am Chem Soc 127:14988–14989

    CAS  Google Scholar 

  121. Fillion E, Wilsily A (2006) J Am Chem Soc 128:2774–2775

    CAS  Google Scholar 

  122. d’Augustin M, Palais L, Alexakis A (2005) Angew Chem Int Ed 44:1376–1378

    Google Scholar 

  123. Fuchs N, d’Augustin M, Humam M, Alexakis A, Taras R, Gladiali S (2005) Tetrahedron: Asymmetry 16:3143–3146

    CAS  Google Scholar 

  124. Mauleón P, Carretero JC (2005) Chem Commun:4961–4963

    Google Scholar 

  125. Takaya Y, Ogasawara M, Hayashi T, Sakai M, Miyaura N (1998) J Am Chem Soc 120:5579–5580

    CAS  Google Scholar 

  126. Hayashi T, Yamasaki K (2003) Chem Rev 103:2829–2844

    CAS  Google Scholar 

  127. Shi Q, Xu L, Li X, Jia X, Wang R, Au-Yeung TTL, Chan ASC, Hayashi T, Cao R, Hong M (2003) Tetrahedron Lett 44:6505–6508

    CAS  Google Scholar 

  128. Boñaga LVR, Krafft ME (2004) Tetrahedron 60:9795–9833

    Google Scholar 

  129. Kwong FY, Li YM, Lam WH, Qiu L, Lee HW, Yeung CH, Chan KS, Chan ASC (2005) Chem Eur J 11:3872–3880

    CAS  Google Scholar 

  130. Lindström UM (2002) Chem Rev 102:2751–2772, and references therein

    Google Scholar 

  131. Kwong FY, Lee HW, Qiu L, Lam WH, Li YM, Kwong HL, Chan ASC (2005) Adv Synth Catal 347:1750–1754

    CAS  Google Scholar 

  132. Culkin DA, Hartwig JF (2003) Acc Chem Res 36:234–245

    CAS  Google Scholar 

  133. Fuji K (1993) Chem Rev 93:2037–2066

    CAS  Google Scholar 

  134. Bolm C, Hildebrand JP, Muñiz K, Hermanns N (2001) Angew Chem Int Ed 40:3284–3308

    CAS  Google Scholar 

  135. Åhman J, Wolfe JP, Troutman MV, Palucki M, Buchwald SL (1998) J Am Chem Soc 120:1918–1919

    Google Scholar 

  136. Hamada T, Chieffi A, Åhman J, Buchwald SL (2002) J Am Chem Soc 124:1261–1268

    CAS  Google Scholar 

  137. Chen G, Kwong FY, Chan HO, Yu WY, Chan ASC (2006) Chem Commun:1413–1415

    Google Scholar 

  138. Drent E, Van Broekhoven JAM, Doyle MJ (1991) J Organomet Chem 417:235–251

    CAS  Google Scholar 

  139. Batistini A, Consiglio G (1992) Organometallics 11:1766–1769

    CAS  Google Scholar 

  140. Barsacchi M, Batistini A, Consiglio G, Sutter UW (1992) Macromolecules 25:3604–3606

    CAS  Google Scholar 

  141. Sen A (1993) Acc Chem Res 26:303–310

    CAS  Google Scholar 

  142. Drent E, Budzelaar PHM (1996) Chem Rev 96:663–682

    CAS  Google Scholar 

  143. Sommazzi A, Garbassi F (1997) Prog Polym Sci 22:1547–1605

    CAS  Google Scholar 

  144. Bianchini C, Meli A (2002) Coord Chem Rev 225:35–66

    CAS  Google Scholar 

  145. Nozaki K, Sato N, Takaya H (1995) J Am Chem Soc 117:9911–9912

    CAS  Google Scholar 

  146. Green MJ, Lucy AR, Lu S, Paton RM (1994) J Chem Soc Chem Commun:2063–2064

    Google Scholar 

  147. Nozaki K, Sato N, Tonomura Y, Yasutomi M, Takaya H, Hiyama T, Matsubara T, Koga N (1997) J Am Chem Soc 119:12779–12795

    CAS  Google Scholar 

  148. Fujita T, Nakano K, Yamashita M, Nozaki K (2006) J Am Chem Soc 128:1968–1975

    CAS  Google Scholar 

  149. Jiang Z, Sen A (1995) J Am Chem Soc 117:4455–4467

    CAS  Google Scholar 

  150. Jiang Z, Adams SE, Sen A (1994) Macromolecules 27:2694–2700

    CAS  Google Scholar 

  151. Bronco S, Consiglio G (1996) Macromol Chem Phys 197:355–365

    CAS  Google Scholar 

  152. Cui Y, Wang L, Kwong FY, Tse MK, Chan ASC (2009) Synlett 16:2696–2700

    Google Scholar 

  153. Cheung HY, Yu WY, Au-Yeung TTL, Zhou Z, Chan ASC (2009) Adv Synth Catal 351:1412–1422

    CAS  Google Scholar 

  154. Trost BM, Crawley ML (2003) Chem Rev 103:2921–2944

    CAS  Google Scholar 

  155. Tusji J (2004) Wiley, New York

    Google Scholar 

  156. Shu C, Hartwig JF (2004) Angew Chem Int Ed 43:4794–4797

    CAS  Google Scholar 

  157. Fisher C, Defieber C, Suzuki T, Carreira EM (2004) J Am Chem Soc 126:1628–1629

    Google Scholar 

  158. López F, Ohmura T, Hartwig JF (2003) J Am Chem Soc 125:3426–3427

    Google Scholar 

  159. Lyothier I, Defieber C, Carreira EM (2006) Angew Chem Int Ed 45:6204–6207

    CAS  Google Scholar 

  160. Welter C, Dahnz A, Brunner B, Streiff S, Dubon P, Helmchen G (2005) Org Lett 7:1239–1242

    CAS  Google Scholar 

  161. Trost BM, Toste FD (1999) J Am Chem Soc 121:4545–4554

    CAS  Google Scholar 

  162. Trost BM, Shen HC, Dong L, Surivet JP (2003) J Am Chem Soc 125:9276–9277

    CAS  Google Scholar 

  163. Trost BM, Toste FD (1998) J Am Chem Soc 120:815–816

    CAS  Google Scholar 

  164. Trost BM, Toste FD (2000) J Am Chem Soc 122:11262–11263

    CAS  Google Scholar 

  165. Haight AR, Stoner EJ, Peterson MJ, Grover VK (2003) J Org Chem 68:8092–8096

    CAS  Google Scholar 

  166. Kimura M, Uozumi Y (2007) J Org Chem 72:707–714

    CAS  Google Scholar 

  167. Uozumi Y, Kimura M (2006) Tetrahedron: Asymmetry 17:161–166

    CAS  Google Scholar 

  168. Tietze LF, Lohmann JK, Stadler C (2004) Synlett 6:1113–1116

    Google Scholar 

  169. Iourtchenko A, Sinou D (1997) J Mol Catal A 122:91–93

    CAS  Google Scholar 

  170. Kim H, Lee C (2002) Org Lett 4:4369–4371

    CAS  Google Scholar 

  171. Pocker Y, Page JD (1990) J Biol Chem 265:22101–22108

    CAS  Google Scholar 

  172. Parkin G (2000) Chem Commun:1971–1985 and references therein

    Google Scholar 

  173. Lam FL, Au-Yeung TTL, Kwong FY, Zhou ZY, Wong KY, Chan ASC (2008) Angew Chem Int Ed 47:1280–1283

    CAS  Google Scholar 

  174. Hansch C, Leo A, Taft RW (1991) Chem Rev 91:165–195

    CAS  Google Scholar 

  175. Gordon AJ, Ford RA (1972) Wiley, New York

    Google Scholar 

  176. Jacobsen EN, Zhang W, Güler ML (1991) J Am Chem Soc 113:6703–6704

    CAS  Google Scholar 

  177. Zhang HC, Xue F, Mak TCW, Chan KS (1996) J Org Chem 61:8002–8003

    CAS  Google Scholar 

  178. Lo MMC, Fu GC (1998) J Am Chem Soc 120:10270–10271

    CAS  Google Scholar 

  179. Doucet H, Fernández E, Layzell TP, Brown JM (1999) Chem Eur J 5:1320–1330

    CAS  Google Scholar 

  180. Lo WC, Che CM, Cheng KF, Mak TCW (1997) Chem Commun:1205–1206

    Google Scholar 

  181. Kwong FY, Yang Q, Mak TCW, Chan ASC, Chan KS (2002) J Org Chem 67:2769–2777

    CAS  Google Scholar 

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Acknowledgment

We thank the Research Grants Council of Hong Kong (CERG: PolyU5001/07P) and the University Grants Committee Areas of Excellence Scheme (AoE/P-10/01) for financial support. Fuk Loi Lam is grateful to the PolyU Postdoctoral Fellowship (G-YX1L).

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Correspondence to Albert S. C. Chan .

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Lam, F.L., Kwong, F.Y., Chan, A.S.C. (2011). Chiral Phosphorus Ligands with Interesting Properties and Practical Applications. In: Ma, S. (eds) Asymmetric Catalysis from a Chinese Perspective. Topics in Organometallic Chemistry, vol 36. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-19472-6_2

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