Highly EnantioselectiveMethanolysis ofMeso-Cyclic Anhydride Mediated by Bifunctional Thiourea Cinchona Alkaloid Derivatives: Access to Asymmetric Total Synthesis of (+)-Biotin-Reference-Cited by-同舟云学术

Highly EnantioselectiveMethanolysis ofMeso-Cyclic Anhydride Mediated by Bifunctional Thiourea Cinchona Alkaloid Derivatives: Access to Asymmetric Total Synthesis of (+)-Biotin

Published:2013-07 Issue: Volume: Page:n/a-n/a
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J Hetercycl Chem

Author:

Xiong Fei,Xiong Fang-Jun¹,Chen Wen-Xue¹,Jia Hui-Qing¹,Chen Fen-Er

Affiliation:

1. Fudan-DSM Joint Lab for Synthetic Method and Chiral Technology, Department of Chemistry; Fudan University; Shanghai; 200433; China

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.1512/fullpdf

Reference13 articles.

1. Biotin: A Timeless Challenge for Total Synthesis

2. Biological significance and development of practical synthesis of biotin

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

4. Total synthesis of (+)-biotin via a quinine-mediated asymmetric alcoholysis of meso-cyclic anhydride strategy

5. Synthetic Studies on (+)‐Biotin, Part 11: Application ofCinchonaAlkaloid‐Mediated Asymmetric Alcoholysis ofmeso‐Cyclic Anhydride in the Total Synthesis of (+)‐Biotin

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