Synthetic Studies ond-Biotin, Part 8:[1] An Efficient Chemoenzymatic Approach to the Asymmetric Total Synthesis ofd-Biotinvia a Polymer-Supported PLE-Mediated Desymmetrization ofmeso-Symmetic Dicarboxylic Esters-Reference-Cited by-同舟云学术

Synthetic Studies ond-Biotin, Part 8:[1] An Efficient Chemoenzymatic Approach to the Asymmetric Total Synthesis ofd-Biotinvia a Polymer-Supported PLE-Mediated Desymmetrization ofmeso-Symmetic Dicarboxylic Esters

Published:2005-03 Issue:4 Volume:347 Page:549-554
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Advanced Synthesis & Catalysis

Author:

Chen Fen-Er,Chen Xu-Xiang,Dai Hui-Fang,Kuang Yun-Yan,Xie Bin,Zhao Jian-Feng

Publisher

Wiley

Subject

General Chemistry

Reference40 articles.

1. Synthetic studies on d-biotin. Part 7: A practical asymmetric total synthesis of d-biotin via enantioselective reduction of meso-cyclic imide catalyzed by oxazborolidine

2. Biotin: A Timeless Challenge for Total Synthesis

3. Encyclopedia of Chemical Technology, Vol 24, (Eds.: R.?E. Kirk, D.?E. Othmer), Wiley, New York, 1984, 41.

4. Highly enantioselective reduction of meso-1,2-dicarboxylic anhydrides

5. A Formal Catalytic Asymmetric Synthesis of (+)-Biotin with Modified Cinchona Alkaloids

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