化学
烷基化
去甲基化
吗啡
立体化学
同种类的
可待因
组合化学
药物化学
有机化学
催化作用
药理学
医学
生物化学
基因表达
热力学
物理
DNA甲基化
基因
作者
Sándor Hosztafi,Csaba Simon,Sándor Makleit
标识
DOI:10.1080/00397919208021649
摘要
Abstract A fews representatives (1b-d) of a novel group of structurally related morphine-antagonist compounds have been prepared in stereochemically homogeneous form. The employed procedures involve O-demethylation either of the corresponding codeine derivatives 2b-d, or those of the N-alkylated analogues 2b-c synthesized from N-demethylthebaine (7a) by means of N-alkylation and subsequent transformations of 7b, d–compounds selected from the resulting functionalized thebaines 7b-exs.
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