GAMMA-LACTAM ANALOGS OF CARBAPENEMS

被引：54

作者：

BOYD, DB ^{[1
]}

FOSTER, BJ ^{[1
]}

HATFIELD, LD ^{[1
]}

HORNBACK, WJ ^{[1
]}

JONES, ND ^{[1
]}

MUNROE, JE ^{[1
]}

SWARTZENDRUBER, JK ^{[1
]}

机构：

[1] ELI LILLY & CO,LILLY RES LAB,LILLY CORP CTR,INDIANAPOLIS,IN 46285

来源：

TETRAHEDRON LETTERS | 1986年 / 27卷 / 30期

关键词：

D O I：

10.1016/S0040-4039(00)84821-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3457 / 3460

页数：4

共 13 条

[1] GAMMA-LACTAM ANALOGS OF PENICILLANIC AND CARBAPENICILLANIC ACIDS [J].

BALDWIN, JE ;

CHAN, MF ;

GALLACHER, G ;

MONK, P ;

PROUT, K .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1983, (05) :250-252

[2] GAMMA-LACTAM ANALOGS OF PENICILLANIC AND CARBAPENICILLANIC ACIDS [J].

BALDWIN, JE ;

CHAN, MF ;

GALLACHER, G ;

OTSUKA, M ;

MONK, P ;

PROUT, K .

TETRAHEDRON, 1984, 40 (21) :4513-4525

[3] GAMMA-LACTAM ANALOGS OF CARBAPENICILLANIC ACIDS [J].

BALDWIN, JE ;

ADLINGTON, RM ;

JONES, RH ;

SCHOFIELD, CJ ;

ZAROCOSTAS, C ;

GREENGRASS, CW .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (04) :194-196

[4]

Boyd D. B., 1982, CHEM BIOL BETA LACTA, V1, P437

[5] FROM PENICILLIN TO PENEM AND CARBAPENEM .5. SYNTHESIS OF CARBAPENAM SKELETON BY (3+2) CYCLIZATION [J].

FUJIMOTO, K ;

IWANO, Y ;

HIRAI, K .

TETRAHEDRON LETTERS, 1984, 25 (11) :1151-1154

[6]

GALE EF, 1981, MOL BASIS ANTIBIOTIC, P79

[7]

HORNBACK WJ, UNPUB

[8]

KAMETANI T, 1983, CHEM PHARM BULL, V31, P2578

[9] AN ALTERNATIVE APPROACH TO THE SYNTHESIS OF THE CARBAPENAM RING-SYSTEM - ALLENES AS ACCEPTOR-DONOR REAGENTS IN 3 + 2 ANNELATIONS [J].

MASTALERZ, H ;

VINET, V .

TETRAHEDRON LETTERS, 1985, 26 (36) :4315-4318

[10]

Merck & Co, 1984, [No title captured], Patent No. [US4428960, 4428960]

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