A NOVEL AND EFFICIENT SYNTHESIS OF THE KEY INTERMEDIATE OF 1-BETA-METHYLCARBAPENEM ANTIBIOTICS FROM (S)-METHYL 3-HYDROXY-2-METHYLPROPIONATE

被引：50

作者：

KAWABATA, T

KIMURA, Y

ITO, Y

TERASHIMA, S

SASAKI, A

SUNAGAWA, M

机构：

[1] SAGAMI CHEM RES CTR,SAGAMIHARA,KANAGAWA 229,JAPAN

[2] SUMITOMO PHARMACEUT CO LTD,DIV RES & DEV,RES LABS,KONOHANA KU,OSAKA 554,JAPAN

来源：

TETRAHEDRON LETTERS | 1986年 / 27卷 / 51期

关键词：

D O I：

10.1016/S0040-4039(00)85442-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：6241 / 6244

页数：4

共 23 条

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[5] COREY EJ, 1979, TETRAHEDRON LETT, P399
[6] LEWIS ACID MEDIATED CONDENSATION OF CHIRAL IMIDE ENOLATES - A GENERAL-APPROACH TO THE SYNTHESIS OF CHIRAL CARBAPENEM PRECURSORS
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[7] GREEN TW, 1981, PROTECTIVE GROUPS OR, P10
[8] AN ENANTIOSELECTIVE BETA-LACTAM SYNTHESIS STARTING FROM L-(S)-GLYCERALDEHYDE ACETONIDE
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[J]. HELVETICA CHIMICA ACTA, 1983, 66 (07) : 2206 - 2209
[9] SIMPLE, STEREOCONTROLLED SYNTHESIS OF 1-BETA-METHYLCARBAPENEM ANTIBIOTICS FROM 3(R)-HYDROXYBUTYRIC ACID
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[J]. TETRAHEDRON LETTERS, 1986, 27 (19) : 2149 - 2152
[10] ITO Y, UNPUB TETRAHEDRON

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