Synthesis of New Cephamycin Derivatives and a Novel Rearrangement between Isothiazolethioacetamides and 1, 3-Dithietanecarboxamides

A novel intramolecular rearrangement of isothiazolethioacetamides into 1, 3-dithietanecarboxamides is described, together with the synthesis of a new cephamycin derivative (YM-09330) having a 1, 3-dithietane structure at the 7β-position. This compound showed strong antibacterial activity, especially...

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Veröffentlicht in:Chemical & pharmaceutical bulletin 1980/09/25, Vol.28(9), pp.2629-2636
Hauptverfasser: IWANAMI, MASARU, MAEDA, TETSUYA, FUJIMOTO, MASAHARU, NAGANO, YOSHINOBU, NAGANO, NORIAKI, YAMAZAKI, ATSUKI, SHIBANUMA, TADAO, TAMAZAWA, KAZUHARU, YANO, KUNIICHIRO
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Sprache:eng
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Zusammenfassung:A novel intramolecular rearrangement of isothiazolethioacetamides into 1, 3-dithietanecarboxamides is described, together with the synthesis of a new cephamycin derivative (YM-09330) having a 1, 3-dithietane structure at the 7β-position. This compound showed strong antibacterial activity, especially against gram-negative organisms.
ISSN:0009-2363
1347-5223
DOI:10.1248/cpb.28.2629