Chemical Communications
The first enantioselective synthesis of cytotoxic marine natural product palau'imide and assignment of its C-20 stereochemistry
HQ Lan, YP Ruan, PQ Huang
Index: Lan, Hong-Qiao; Ruan, Yuan-Ping; Huang, Pei-Qiang Chemical Communications, 2010 , vol. 46, # 29 p. 5319 - 5321
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Citation Number: 11
Abstract
Methyl tetramate derivative 6 has been developed as a new building block for the flexible and racemization-free synthesis of methyl 5-benzyl-3-methyltetramate via alkylation, and used in the first asymmetric synthesis of palau'imide (1). This allowed the establishment of the hitherto unknown stereochemistry at the C-20 of palau'imide as S.
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