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Nat Prod Res ; 36(21): 5416-5422, 2022 Nov.
Article in English | MEDLINE | ID: mdl-34157905

ABSTRACT

The total synthesis of Benzannulated macrolide, (+)-Xestodecalactone A was accomplished starting from commercially available enantiomerically pure propylene oxide and 3,5-dihydroxyphenylacetic acid using Grignard reaction, alkylation of 1,3-dithiane and Yamaguchi macrolactonisation as key steps.


Subject(s)
Lactones , Macrolides , Stereoisomerism , Alkylation
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