EFFICIENT CHIRAL SYNTHESIS OF MELILLOS LACTONE, A KEY INTERMEDIATE FOR THE SYNTHESIS OF THIENAMYCIN

被引：11

作者：

KAMETANI, T

HONDA, T

ISHIZONE, H

KANADA, K

NAITO, K

SUZUKI, Y

机构：

[1] HOSHI UNIV,INST MED CHEM,EBARA 2-4-41,SHINAGAWA KU,TOKYO 142,JAPAN

[2] HORIUCHI ITARO & CO LTD,RES & DEV,HIGASHIMURAYAMA,TOKYO 189,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1989年 / 10期

关键词：

D O I：

10.1039/c39890000646

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：646 / 647

页数：2

共 5 条

[1]

IKOTA N, 1982, CHEM PHARM BULL, V30, P1929

[2] A FACILE SYNTHESIS OF (+)-TECOMANINE USING A CHIRAL CYCLOPENTANE DERIVATIVE [J].

KAMETANI, T ;

SUZUKI, Y ;

BAN, C ;

HONDA, T .

HETEROCYCLES, 1987, 26 (06) :1491-1493

[3] A FORMAL SYNTHESIS OF N-ACETYL-L-ACOSAMINE [J].

KAMETANI, T ;

SUZUKI, Y ;

BAN, C ;

KANADA, K ;

HONDA, T .

HETEROCYCLES, 1987, 26 (07) :1789-1792

[4] FURTHER-STUDIES ON THE ACETONEDICARBOXYLATE ROUTE TO THIENAMYCIN - STEREOCHEMICAL INVERSION AT THE LACTONE STAGE [J].

MELILLO, DG ;

LIU, T ;

RYAN, K ;

SLETZINGER, M ;

SHINKAI, I .

TETRAHEDRON LETTERS, 1981, 22 (10) :913-916

[5]

NAGAHARA T, 1987, HETEROCYCLES, V25, P729

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