氮杂环丁烷
林可酰胺
化学
立体化学
烷基
烷基化
戒指(化学)
有机化学
抗生素
生物化学
克林霉素
催化作用
作者
Hardwin O’Dowd,Jason G. Lewis,Joaquim Trias,Rumi Asano,Johanne Blais,Sara López,Craig K. Park,Charlotte Wu,Wen Wang,M. F. GORDEEV
标识
DOI:10.1016/j.bmcl.2008.03.032
摘要
The synthesis and evaluation of novel azetidine lincosamides 1 are described. Eleven new (3-trans-alkyl)azetidine-2-carboxylic acids were synthesized via alkylation of N-TBS-4-oxo-azetidine-2-carboxylic acid and subsequent elaboration then coupled to 7-chloro-1-methylthio-lincosamine. The resulting lincosamides differ from the drug clindamycin in both the size of the ring and the position/structure of the alkyl side-chain. SAR within the series was explored with attention to alkyl variants in positions 1 and 3 of the azetidine ring.
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