Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers

  • Syuzanna R. Harutyunyan

Part of the Topics in Organometallic Chemistry book series (TOPORGAN, volume 58)

Table of contents

  1. Front Matter
    Pages i-vii
  2. Valentín Hornillos, Jean-Baptiste Gualtierotti, Ben L. Feringa
    Pages 1-39
  3. Pablo Ortiz, Francesco Lanza, Syuzanna R. Harutyunyan
    Pages 99-134
  4. Alexander Hensel, Martin Oestreich
    Pages 135-167
  5. Xiaofeng Wei, Yohei Shimizu, Motomu Kanai
    Pages 169-182
  6. Xin Fang, Jia-Wei Zhang, Chun-Jiang Wang
    Pages 183-205
  7. Andrei V. Malkov, Kurt Lawson
    Pages 207-220
  8. Back Matter
    Pages 221-224

About this book


The series Topics in Organometallic Chemistry presents critical overviews of research results in organometallic chemistry. As our understanding of organometallic structure, properties and mechanisms increases, new ways are opened for the design of organometallic compounds and reactions tailored to the needs of such diverse areas as organic synthesis, medical research, biology and materials science. Thus the scope of coverage includes a broad range of topics of pure and applied organometallic chemistry, where new breakthroughs are being achieved that are of significance to a larger scientific audience. The individual volumes of Topics in Organometallic Chemistry are thematic. Review articles are generally invited by the volume editors. All chapters from Topics in Organometallic Chemistry are published OnlineFirst with an individual DOI. In references, Topics in Organometallic Chemistry is abbreviated as Top Organomet Chem and cited as a journal.


Addition-cyclisation reactions Aldehydes Asymmetric allylic substitution Boron nucleophiles Grignard reagents Organolithium reagents Quaternary stereogenic centers Silicon nucleophiles Soft carbon nucleophiles Symmetric addition

Editors and affiliations

  • Syuzanna R. Harutyunyan
    • 1
  1. 1.Stratingh Institute for ChemistryUniversity of GroningenGroningenThe Netherlands

Bibliographic information

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