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Title:
OPTICALLY ACTIVE CEPHALOSPORIN ANALOG
Document Type and Number:
Japanese Patent JPS55108872
Kind Code:
A
Abstract:

NEW MATERIAL:Optically active cephalosporin analogs of formula I (R1 is H, lower alkyl; R2 is H, residual group of ester hydrogen atoms in the 6 and 7 positions are in cis configuration.) and their salts.

EXAMPLE: (+)-7β-Amino-1-azabicyclo[4,2,0]oct-2-ene-8-one-2-carboxylic acid.

USE: Antibiotic; the acylated compounds show very strong antibacterial activity compared with the corresponding inactive derivative.

PREPARATION: The compound of formula II (R is substituted or unsubstituted unsaturated carbon-six-membered or hetero-5-membered ring; X is H, amino, hydroxyl, lower alkyl) is subjected to optically active deacylation using a microorganism belonging to Aeromonas and only the one of optically active enantiomers is separated in high yield. This process is quite new.


Inventors:
HIRATA TADASHI
HASHIMOTO YUKIO
OGASA TAKEHIRO
KOBAYASHI SHIGERU
MATSUKUMA MASAO
KIMURA KAZUO
Application Number:
JP1453379A
Publication Date:
August 21, 1980
Filing Date:
February 10, 1979
Export Citation:
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Assignee:
KYOWA HAKKO KOGYO KK
International Classes:
C07D463/00; A61K31/435; C07D471/04; C12P35/00; C12P41/00; C12R1/02; (IPC1-7): A61K31/435; C07D471/04; C12P35/00; C12R1/02