ALDOL ADDITION-REACTION OF CHIRAL ACETYLUREA AND A CONVENIENT SYNTHESIS OF OPTICALLY PURE METHYL BETA-ALKYL-BETA-HYDROXYPROPIONATE

被引：14

作者：

KISHIKAWA, K ^{[1
]}

YAMAMOTO, M ^{[1
]}

KOHMOTO, S ^{[1
]}

YAMADA, K ^{[1
]}

机构：

[1] CHIBA UNIV, DEPT IND CHEM, CHIBA 260, JAPAN

来源：

CHEMISTRY LETTERS | 1989年 / 05期

关键词：

D O I：

10.1246/cl.1989.787

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：787 / 790

页数：4

共 10 条

[1]

FATER G, 1979, HELV CHIM ACTA, V62, P2825

[2] STEREOSPECIFIC SYNTHESIS OF (+)-(3R,4R)-4-METHYL-3-HEPTANOL - ENANTIOMER OF A PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE (SCOLYTUS-MULTISTRIATUS) [J].

FRATER, G .

HELVETICA CHIMICA ACTA, 1979, 62 (08) :2829-2832

[3] DIELS-ALDER REACTION OF CHIRAL ACRYLAMIDE AND A CONVENIENT SYNTHESIS OF OPTICALLY PURE METHYL (3R,4R,6R)-BICYCLO[2.2.1]HEPTENE-4-CARBOXYLATE [J].

KISHIKAWA, K ;

YAMAMOTO, M ;

KOHMOTO, S ;

YAMADA, K .

CHEMISTRY LETTERS, 1988, (10) :1623-1624

[4]

KISHIKAWA K, 1989, IN PRESS J ORG CHEM

[5]

KRAUS GA, 1977, TETRAHEDRON LETT, P4575

[6]

PIRCLE WH, 1983, ASYMMETRIC SYNTHESIS, V1, P89

[7]

SCHOPF C, 1959, LIEBIGS ANN CHEM, V626, P150

[8] PREPARATION OF OPTICALLY-ACTIVE ALCOHOLS FROM 1,3-DIOXAN-4-ONES - A PRACTICAL VERSION OF THE ASYMMETRIC-SYNTHESIS WITH NUCLEOPHILIC-SUBSTITUTION AT ACETAL CENTERS [J].

SEEBACH, D ;

IMWINKELRIED, R ;

STUCKY, G .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1986, 25 (02) :178-180

[9] STEREOSELECTIVE REARRANGEMENT OF CHIRAL ACYLISOUREAS AND A MODEL FOR THE TRANSITION-STATE [J].

YAMADA, K ;

KISHIKAWA, K ;

KOHMOTO, S ;

YAMAMOTO, M .

CHEMISTRY LETTERS, 1988, (02) :351-352

[10] 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

← 1 →