期刊
ORGANIC LETTERS
卷 13, 期 16, 页码 4252-4255出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol201604c
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资金
- Department of Science and Technology (DST), New Delhi
- Council of Scientific and Industrial Research (CSIR), New Delhi
Enantioselective formal synthesis of macrolactone palmerolide A, a polyketide marine natural product, is described. Key strategies in the synthesis include the oxidative furan ring-opening of a chiral furyl carbinol for the installation of the 1,4-dienol core and a Jung nonaldol-aldol reaction for the dienamide core.
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