FUNCTIONALIZATION OF PENICILLINS AT CARBON 6 VIA N-ACYLIMINES - 6-HYDROXYPENICILLIN - SUBSTITUTED PENICILLINS AND CEPHALOSPORINS .8.

被引：46

作者：

FIRESTONE, RA ^{[1
]}

CHRISTENSEN, BG ^{[1
]}

机构：

[1] MERCK SHARP & DOHME, RES LABS, RAHWAY, NJ 07065 USA

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1973年 / 38卷 / 07期

关键词：

D O I：

10.1021/jo00947a051

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：1436 / 1437

页数：2

共 11 条

[1]

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CAMA, LD ;

BEATTIE, TR ;

LEANZA, WJ ;

CHRISTEN.BG .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (04) :1408-&

[3]

CAMA LD, TO BE PUBLISHED

[4]

FIRESTONE RA, 1972, TETRAHEDRON LETT, P375

[5]

JOHNSTON DB, 1972, TETRAHEDRON LETT, P4917

[6]

MILLER AK, 1972, ANTIMICROB AGENTS CH, V2, P281, DOI 10.1128/AAC.2.4.281

[7] CEPHAMYCINS, A NEW FAMILY OF BETA-LACTAM ANTIBIOTICS .2. ISOLATIN AND CHEMICAL CHARACTERIZATION [J].

MILLER, TW ;

WOLF, FJ ;

WESTON, RG ;

GOEGELMAN, RT ;

PUTTER, I .

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1972, 2 (03) :132-+

[8] SUBSTITUTION OF 6-AMINOPENICILLANIC ACID AT CARBON 6 [J].

REINER, R ;

ZELLER, P .

HELVETICA CHIMICA ACTA, 1968, 51 (08) :1905-&

[9]

SHEEHAN JC, 1964, MOLECULAR MODIFICATI, P22

[10]

SPITZER WA, 1972, CHEM COMMUN, P1139

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