KOH, HY KANG, HY CHOI, KI CHANG, MH 2024-01-22T00:10:46Z 2024-01-22T00:10:46Z 2022-01-11 1990-12-20 0253-2964 https://pubs.kist.re.kr/handle/201004/147009 New aminothiazolyl cephalosporins with alkoxyiminomethyl(2-aminothiazol-4-yl)acetyl substituents at 7-position of cephems were synthesized starting from (2-aminothiazol-4-yl)acetate via one carbon homologation followed by acylation with 7-aminoceph-3-em-4-carboxylic acid derivatives. These new aminothiazolyl cephalosporins exhibit promising in vitro activities against various strains including Gram positive bacteria. English KOREAN CHEMICAL SOC NEW AMINOTHIAZOLYL CEPHALOSPORINS - SYNTHESIS AND BIOLOGICAL EVALUATION OF 7-[ALKOXYIMINOMETHYL(2-AMINOTHIAZOL-4-YL)ACETAMIDO]CEPH-3-EM-4-CARBOXYLI C ACIDS Article 1 BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.11, no.6, pp.538 - 542 BULLETIN OF THE KOREAN CHEMICAL SOCIETY 11 6 538 542 scie A1990EV68600022 Chemistry, Multidisciplinary Chemistry Article