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SYNTHESIS OF HIGHLY STEREOSELECTIVE BETA-LACTAM DERIVATIVE

机译:高度立体选择性β-内酰胺衍生物的合成

摘要

PURPOSE: To efficiently obtain the derivative useful for thienamycin in a high yield by reacting an organic ester lithium enolate with a specific organic imine compound in THF. ;CONSTITUTION: The lithium enolate of an organic ester such as β-hydroxybutyric acid ethyl ester is reacted with an organic imine compound such as an imine coordinated with a trialkylaluminum in THF to obtain this derivative.;COPYRIGHT: (C)1994,JPO&Japio
机译:目的:通过使有机酯烯酸锂与特定的有机亚胺化合物在THF中反应,以高收率高效地获得可用于硫霉素的衍生物。组成:将有机酯(如β-羟基丁酸乙酯)的烯醇锂与有机亚胺化合物(如与三烷基铝配位的亚胺)在THF中反应制得该衍生物。版权所有:(C)1994,JPO&Japio

著录项

  • 公开/公告号JPH0656770A

    专利类型

  • 公开/公告日1994-03-01

    原文格式PDF

  • 申请/专利权人 TOYO SUTOUFUAA CHEM:YUGEN;

    申请/专利号JP19910125207

  • 发明设计人 NAKAI SHUICHI;KOKUNI NOBUKI;

    申请日1985-10-02

  • 分类号C07D205/08;

  • 国家 JP

  • 入库时间 2022-08-22 04:48:00

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