Total Synthesis of the Putative Structure of Lucentamycin A
收藏NIAID Data Ecosystem2026-03-06 收录
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资源简介：
A rapid and stereoselective enolate-Claisen rearrangement provides access to the 4-ethylidene-3-methylproline (Emp) subunit of lucentamycin A. Synthesis of the putative structure of the cytotoxic natural product suggests the need for structural revision.
创建时间：
2016-02-25
