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filingDate 1965-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14f03c889f0f53e1235adc1d90882e0b
publicationDate 1970-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-497456-A
titleOfInvention Process for the preparation of azetidino (3,2-d) thiazolidine compounds
abstract 4, 4.disubstituted 3-R1 2-oxoacetidine(3.2-d) thiazolidine compounds of general formula (I) R1 = H or preferably an acyl group; X = the disubstituted C-atom of the thiazolidine ring, especially a group of formula (2) (2) R2 and R3=hydrocarbon residues especially aliphatic hydrocarbons such as alkyl- groups, preferably methyl; aromatic groups especially phenyl groups, araliphatic hydrocarbons, especially phenylalkyl groups; and functionally modified especially esterified carboxy groups. R2 + R3 may form a bivalent, preferably aliphatic hydrocarbon such as an alkylene group; a phthaloyl-, oxo- or thiono group. The hydrocarbon groups may be substituted with alkyl, alkoxy, halogen, halogenalkyl or other suitable groups.
priorityDate 1965-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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