Highly efficient and general method for synthesis of tertiary allylic alcohols in a chiral form. Synthesis of arbaprostil
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. S. Okamoto, H. Tsujiyama, T. Yoshimo, and F. Sato, Tetrahedron Lett., preceding paper.
2. A practical, efficient method for preparation of four possible stereoisomers of secondary allylic alcohols using kinetic resolution of (E)-1-trimethylsilylalk-1-en-3-ol by the sharpless process
3. A highly efficient kinetic resolution of γ- and β- trimethylsilyl secondary allylic alcohols by the sharpless asymmetric epoxidation
4. Structure-activity studies of 16-methoxy-16-methyl prostaglandins
5. Asymmetric alkylation of an α-keto ester with chiral lithium alkoxy-tributylaluminates
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