Author:
Yu Xiao-Ming,Bian Chuan-Cai,Li Yong-Qiang,Yang Hao-ran
Abstract
AbstractA route for the scalable, stereocontrolled, total synthesis of carolacton is presented starting from commercially available S-Roche ester, d-ribose, and a known allylic alcohol. Key transformations in the total synthesis include a [3,3]-Claisen rearrangement, Sharpless asymmetric epoxidation–methyl ring-opening, or Leighton asymmetric crotylation, Evans aldol–reductive deoxygenation, and ring closing metathesis (RCM). The total synthesis of carolacton (151 mg isolated, 9.2% overall yield) was completed in 23 linear steps. Additionally, 56 mg of the carolacton C15–C16 cis-olefin isomer was obtained.
Funder
National Natural Science Foundation of China
CAMS Innovation Fund for Medical Sciences
Subject
Organic Chemistry,Catalysis
Cited by
1 articles.
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