ALKYLATION OF AMINO-ACIDS WITHOUT LOSS OF OPTICAL-ACTIVITY - ALPHA-ALKYLATION AND BETA-ALKYLATION OF AN ASPARTIC-ACID DERIVATIVE

被引：109

作者：

SEEBACH, D

WASMUTH, D

机构：

来源：

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1981年 / 20卷 / 11期

关键词：

D O I：

10.1002/anie.198109711

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：971 / 971

页数：1

共 17 条

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[12] PREPARATION FOR ERYTHRO-2-HYDROXY-SUCCINIC ACID-DERIVATIVES FROM MALIC ESTERS [J].

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[13] METHODS OF REACTIVITY UMPOLUNG [J].

SEEBACH, D .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1979, 18 (04) :239-258

[14] ON STEREOCHEMICAL COURSE OF ELECTROPHILIC SUBSTITUTION AT CH GROUPS IN ALPHA-POSITION TO N-ATOM OF HINDERED AMIDES [J].

SEEBACH, D ;

LUBOSCH, W ;

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KALINOWSKI, HO .

HELVETICA CHIMICA ACTA, 1978, 61 (08) :3100-3102

[15]

Seebach D., 1979, ANGEW CHEM, V91, P259

[16]

SEEBACH D, 1981, ANGEW CHEM, V93, P422

[17] 2,3-DISUBSTITUTED GAMMA-BUTYROLACTAMS FROM THE MICHAEL-ADDITIONS OF DOUBLY DEPROTONATED, OPTICALLY-ACTIVE BETA-HYDROXYCARBOXYLATES TO NITROOLEFINS [J].

ZUGER, M ;

WELLER, T ;

SEEBACH, D .

HELVETICA CHIMICA ACTA, 1980, 63 (07) :2005-2009

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