染色质结构重塑复合物
钥匙(锁)
立体选择性
组合化学
化学
抗生素
立体化学
可扩展性
计算机科学
有机化学
生物化学
DNA
数据库
催化作用
计算机安全
组蛋白
核小体
作者
Shinya Hisakawa,Katsuki Yokoo,Shinichiro Hara,Toshiaki Aoki,Jun Sato,Hiroki Kusano,Yoshifumi Kusumoto,Kenji Yamawaki
标识
DOI:10.1021/acs.oprd.5c00111
摘要
Cephalosporins are valuable antibiotics for clinical treatment of infectious diseases. RSC-435830 is a cephalosporin-containing antibiotic with a unique C2 (S)-methylcephalosporin structure. It was a synthetic challenge to construct a chiral methyl group at the C-2 position on the cephalosporin scaffold. We report herein two routes for the stereoselective and scalable synthesis of C2 (S)-methylcephalosporin 4, a key intermediate of RSC-435830, that has advanced to phase I clinical trials. The first route focused on stereoselective isomerization of the double bond on the cephalosporin structure without significant changes from the initial synthetic route. For the second route, we set an alternative starting material and then optimized a Mannich-type reaction followed by stereoselective reduction, to enable shortening of the reaction steps from the first route. This culminated in the synthesis of several hundred grams of the key intermediate 4 leading to RSC-435830.
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