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手性相转移催化 2-甲基苄基叔丁基丙二酸酯的α-烷化反应。

Enantioselective phase-transfer catalytic α-alkylation of 2-methylbenzyl tert-butyl malonates.

机构信息

Research Institute of Pharmaceutical Sciences and College of Pharmacy, Seoul National University, Seoul 151-742, Republic of Korea.

出版信息

Org Biomol Chem. 2013 Jun 28;11(24):4030-9. doi: 10.1039/c3ob40481a.

Abstract

A new asymmetric synthetic method to prepare α,α-dialkylmalonates for the construction of a quaternary carbon center via phase-transfer catalytic (PTC) alkylation has been developed. Enantioselective α-alkylation of 2-methylbenzyl tert-butyl α-methylmalonates under phase-transfer catalytic conditions in the presence of (S,S)-3,4,5-trifluorophenyl-NAS bromide () afforded the corresponding α,α-dialkylmalonates in high chemical (up to 99%) and optical yields (up to 91% ee), which were selectively hydrolyzed to malonic monoacids under alkali basic conditions for conversion to versatile chiral intermediates.

摘要

已开发出一种通过相转移催化(PTC)烷基化来构建季碳原子的新型不对称合成方法,以制备α,α-二烷基丙二酸酯。在(S,S)-3,4,5-三氟苯基-NAS 溴化物()的存在下,通过相转移催化条件对 2-甲基苄基叔丁基α-甲基丙二酸酯进行对映选择性α-烷基化,可高化学收率(高达 99%)和光学收率(高达 91%ee)得到相应的α,α-二烷基丙二酸酯,这些产物在碱性条件下选择性水解为丙二酸单酸,可转化为多功能手性中间体。

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