Synthetic Studies on (+)-Biotin, Part 15: A Chiral Squaramide-Mediated Enantioselective Alcoholysis Approach toward the Total Synthesis of (+)-Biotin
Author:
Affiliation:
1. Fudan-DSM Joint Laboratory for Synthetic Method and Chiral Technology, Department of Chemistry, Fudan University
2. Institutes of Biomedical Sciences, Fudan University
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb/59/4/59_4_488/_pdf
Reference27 articles.
1. A novel synthetic strategy for the stereospecific total synthesis of (±)-biotin
2. Stereoselective Anhydride Openings
3. Asymmetric Alcoholysis of Cyclic Anhydrides
4. Catalysis of the Asymmetric Desymmetrization of Cyclic Anhydrides by Nucleophilic Ring-Opening with Alcohols
5. Highly Enantioselective Desymmetrization of Meso Anhydrides by a Bifunctional Thiourea-Based Organocatalyst at Low Catalyst Loadings and Room Temperature
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