首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Synthesis of the 2 beta,3 beta-, 2 alpha,3 beta-, 2 beta,3 alpha- and 2 alpha,3 alpha- isomers of 6 beta-hydroxy-3-(p-tolyl)tropane-2-carboxylic acid methyl ester
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Synthesis of the 2 beta,3 beta-, 2 alpha,3 beta-, 2 beta,3 alpha- and 2 alpha,3 alpha- isomers of 6 beta-hydroxy-3-(p-tolyl)tropane-2-carboxylic acid methyl ester

机译:6β-羟基-3-(对甲苯基)托烷-2-羧酸的2 beta,3 beta-,2 alpha,3 beta-,2 beta,3 alpha-和2 alpha,3 alpha-异构体的合成甲酯

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摘要

6-Hydroxytropanone (8) was synthesized by a Mannich type condensation between acetonedicarboxylic acid, methylamine hydrochloride, and the hydrolysis product of 2,5-dimethoxydihydrofuran and was used as the key intermediate for the synthesis of the four racemic isomers of 6 beta-hydroxy-2-(methoxycarbonyl)-3-(p-tolyl)tropane. (C) 1999 Elsevier Science Ltd. All rights reserved. [References: 24]
机译:通过丙酮二羧酸,甲胺盐酸盐和2,5-二甲氧基二氢呋喃的水解产物之间的曼尼希式缩合反应合成6-羟基对pan酮(8),并用作合成6个β-羟基的四个外消旋异构体的关键中间体-2-(甲氧基羰基)-3-(对甲苯基)托烷。 (C)1999 Elsevier ScienceLtd。保留所有权利。 [参考:24]

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