A NEW NUCLEOPHILIC ALANINOL SYNTHON FROM SERINE

被引：78

作者：

SIBI, MP

RENHOWE, PA

机构：

[1] Department of Chemistry, North Dakota State University Fargo

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 51期

关键词：

D O I：

10.1016/S0040-4039(00)88501-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A new nucleophilic alaninol synthon derived from serine is reported. The utility of this reagent in the stereoselective synthesis of beta,gamma-unsaturated amino alcohols is described.

引用

页码：7407 / 7410

页数：4

共 32 条

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[2] CONVERSION OF SERINE BETA-LACTONES TO CHIRAL ALPHA-AMINO-ACIDS BY COPPER-CONTAINING ORGANOLITHIUM AND ORGANOMAGNESIUM REAGENTS
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[5] NUCLEOPHILIC RING-OPENING OF AZIRIDINE-2-CARBOXYLATES WITH WITTIG REAGENTS - AN ENANTIOEFFICIENT SYNTHESIS OF UNSATURATED AMINO-ACIDS
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[6] NON-PROTEINOGENIC AMINO-ACID SYNTHESIS - THE BETA-ANION DERIVED FROM ASPARTIC-ACID, AND ITS APPLICATION TO ALPHA-AMINO-ACID SYNTHESIS
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[7] THE RING-OPENING OF AZIRIDINE-2-CARBOXYLATE ESTERS WITH ORGANOMETALLIC REAGENTS
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ONEIL, IA
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[9] ENANTIOSPECIFIC SYNTHESIS OF D-ALPHA,OMEGA-DIAMINOALKANOIC ACIDS
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[J]. TETRAHEDRON LETTERS, 1988, 29 (17) : 2019 - 2022
[10] SYNTHESIS OF ALPHA-AMINO-ACIDS WITH BETA,GAMMA-UNSATURATED SIDE-CHAINS
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