对映选择合成
左炔诺孕酮
形式综合
医学
芯(光纤)
药理学
诺格列酮
立体化学
人口
化学
类固醇
钥匙(锁)
作者
Dražen Pavlović,Daniel F A R Dourado,Andrew S. Rowan,Gareth Brown,Darren Gray,Jenny Spratt,Alexandra T P Carvalho,Jill Caswell,Derek J. Quinn,Sergei Maciuk,Fernando Tur,Stefan Mix,Thomas S. Moody
标识
DOI:10.26434/chemrxiv.15000108/v1
摘要
A concise formal synthesis of levonorgestrel (LNG) precursor, a natural 18a-homoestrone, 13-ethyl-3methoxy-gona-2,5(10)-dien-17-one (11) is described, in which the steroid core of LNG is formed by enantioselective CRED bioreduction of prochiral secodione 4 followed by Torgov cyclization as the key steps.
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