Optically active carbacyclin intermediates and processes for the preparation thereof

Claim 2

A process for preparing a compound of formula (I) ##STR14## wherein R represents lower alkyl and B represents an alkylene group optionally substituted with alkyl, and a compound of formula (III) ##STR15## wherein R and B have the meanings given above, said process comprising treating a (1SR,5RS)-7,7-alkylenedioxy-2-alkoxycarbonyl-cis-bicyclo[3.3.0]octan-3-one, which is a racemic compound of formula (II) ##STR16## wherein R and B have the meanings given above, with a microorganism having an ability of specifically reducing the keto group of the (1R,5S) epimer of the racemic compound (II), thereby giving, as a nonreduced compound, an optically active (1S,5R)-7,7-alylenedioxy-2-alkoxy-carbonyl-bicyclo[3.3.0]octan-3-one of said formula (I) and, as a reduced compound, an optically active (1S,5R,6R,7S)-3,3-alkylenedioxy-7-hydroxy-6-alkoxycarbonylbicyclo [3.3.0] octane of said formula (III), wherein R ad B have the meanings given above.

Claim 3

The process of claim 1 which further comprises separating the compound of the formula (I) or the compound of the formula (III) by ordinary separation techniques.

Claim 4

The process of claim 1 wherein the microorganism for the treatment of the racemic compound is yeast.

Claim 5

The process of claim 3 wherein the yeast includes genera Pichia and Saccharomyces.

Claim 6

The process of claim 4 wherein the yeast includes Saccharomyces cerevisiae, Saccharomyces uvarum, Saccharomyces carlsbergensis, Saccharomyces bailii or Pichia terricola.

Claim 7

A process for converting a compound of formula III ##STR17## wherein R represents lower alkyl and B represents an alkylene group optionally substituted with alkyl, into a compound of formula II ##STR18## wherein R and B have the meanings given above, said process comprising subjecting to an oxidation reaction, an optically active (1S,5R,6R,7S)-3,3-alkylenedioxy-7-hydroxy-6-alkoxycarbonyl-bicyclo [3.3.0] octane of said formula III wherein R and B have the meanings given above, so as to convert the hydroxy group thereof into a keto group, subjecting the thus oxidized compound to saponification and decarboxylation so as to give a 7,7-alkylenedioxy-cis-bicyclo [3.3.0] octan-3-one of formula (IV) ##STR19## wherein B has the meaning given above, and introducing an alkoxycarbonyl group into the 2-position of the compound of formula (IV) to convert into the racemic compound, a (1SR,5RS)-7,7-alkylenedioxy-2-alkoxycarbonyl-cis-bicyclo [3.3.0] octan-3-one of said formula II wherein R and B have the meaning s given above.

Claim 8

A process for converting a compound of formula III ##STR17## wherein R represents lower alkyl and B represents an alkylene group optionally substituted with alkyl, into a compound of formula II ##STR18## wherein R and B have the meanings given above, said process comprising subjecting to an oxidation reaction, an optically active (1S,5R,6R,7S)-3,3-alkylenedioxy-7-hydroxy-6-alkoxycarbonyl-bicyclo [3.3.0] octane of said formula III wherein R and B have the meanings given above, so as to convert the hydroxy group thereof into a keto group, subjecting the thus oxidized compound to saponification and decarboxylation so as to give a 7,7-alkylenedioxy-cis-bicyclo [3.3.0] octan-3-one of formula (IV) ##STR19## wherein B has the meaning given above, and introducing an alkoxycarbonyl group into the 2-position of the compound of formula (IV) to convert into the racemic compound, a (1SR,5RS)-7,7-alkylenedioxy-2-alkoxycarbonyl-cis-bicyclo [3.3.0] octan-3-one of said formula II wherein R and B have the meaning s given above.