Total Synthesis of Okaspirodiol

被引:0
|
作者
Madasu, Madhu [1 ]
Mohapatra, Debendra K. [1 ]
机构
[1] Indian Inst Chem Technol, Dept Organ Synth & Proc Chem, CSIR, Hyderabad 500007, India
来源
CHEMISTRYSELECT | 2023年 / 8卷 / 13期
关键词
Acid-catalyzed spiroketalization; Okaspirodiol; Sharpless asymmetric epoxidation; Spiroketal; Wittig reaction; ENANTIOSELECTIVE SYNTHESIS; BIOLOGICAL-ACTIVITY; SECONDARY ALCOHOLS; NATURAL-PRODUCTS; REVEROMYCIN-A; BIOSYNTHESIS; CHEMISTRY; GROWTH;
D O I
10.1002/slct.202300352
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The asymmetric total synthesis of okaspirodiol was achieved following Sharpless asymmetric epoxidation, Gilman reaction, Wittig reaction, Horner-Wadsworth-Emmons olefination, and coupling of alkyne with the aldehyde, and acid-catalyzed spiroketalization as key reactions.
引用
收藏
页数:7
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