A general route toward 2-oxo-, 2-thioxo- and 2-iminopenams and their conversion into 2-alkoxy-, 2-alkylthio- and 2-aminopenems
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (25) , 2563-2566
- https://doi.org/10.1016/s0040-4039(00)81982-6
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- 2-Thioxopenams, useful intermediated for penem synthesisJournal of the Chemical Society, Chemical Communications, 1982
- Use of the allylic sulphoxide–sulphenate ester rearrangement for the synthesis of a 2-thiacephem and a penemJournal of the Chemical Society, Chemical Communications, 1982
- Synthesis of 2-oxo-bisnorpenicillin G estersTetrahedron Letters, 1980
- 2-(Alkylthio)penem-3-carboxylic acids II. Chemical manipulation of penem side chains.CHEMICAL & PHARMACEUTICAL BULLETIN, 1980
- 2-(Alkylthio)penem-3-carboxylic acids I. Synthesis of 6-unsubstituted penems.CHEMICAL & PHARMACEUTICAL BULLETIN, 1980
- Synthetic studies on β-lactam antibiotics. Part 4. Preparation of -3-acylamino-4-mercaptoazetidin-2-ones by acid hydrolysis of thiazolinoazetidinonesTetrahedron Letters, 1978
- The penems, a new class of .beta.-lactam antibiotics: 6-acylaminopenem-3-carboxylic acidsJournal of the American Chemical Society, 1978