THE RING-OPENING OF AZIRIDINE-2-CARBOXYLATE ESTERS WITH ORGANOMETALLIC REAGENTS

被引：95

作者：

BALDWIN, JE ^{[1
]}

ADLINGTON, RM ^{[1
]}

ONEIL, IA ^{[1
]}

SCHOFIELD, C ^{[1
]}

SPIVEY, AC ^{[1
]}

SWEENEY, JB ^{[1
]}

机构：

[1] OXFORD CTR MOLEC SCI,OXFORD OX1 3QY,ENGLAND

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1989年 / 23期

关键词：

D O I：

10.1039/c39890001852

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1852 / 1854

页数：3

共 14 条

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[3] NUCLEOPHILIC RING-OPENING OF AZIRIDINE-2-CARBOXYLATES WITH WITTIG REAGENTS - AN ENANTIOEFFICIENT SYNTHESIS OF UNSATURATED AMINO-ACIDS
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[6] SUBSTITUTION-REACTIONS OF SECONDARY HALIDES AND EPOXIDES WITH HIGHER-ORDER, MIXED ORGANOCUPRATES, R2CU(CN)LI2 - SYNTHETIC, STEREOCHEMICAL, AND MECHANISTIC ASPECTS
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[7] THE CHEMISTRY OF HIGHER-ORDER ORGANOCUPRATES
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[8] ALPHA-AMINO-ACIDS AS CHIRAL EDUCTS FOR ASYMMETRIC PRODUCTS - CHIROSPECIFIC SYNTHESES OF METHYL L-SIBIROSAMINIDE AND ITS C-3 EPIMER FROM L-ALLOTHREONINE
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