Oxazolines
US4220766A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Jan 10, 1978 |
| Grant date | Sep 2, 1980 |
| Priority date | — |
| Expiry date | Jan 10, 1998 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY02P20/582
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
Abstract
Useful intermediates for preparing a 1-dethia-1-oxacephalosporin and represented by the following formula: ##STR1## (wherein R is a monovalent group resulting from the elimination of the carbonyl function of an acyl group derived from a carboxylic or carbonic acid; PA1 COB is carboxy or protected carboxy; and PA1 X is hydrogen or a nucleophilic group) are prepared from the corresponding penicillin 1-oxides of the following formula: ##STR2## (wherein R, COB, and X are as defined above) by heating, if required in the presence of the desulfurizing reagent, or by exchanging the X group with another one under the condition of an appropriate nucleophilic substitution.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.