Synthesis and biological evaluation of new C (4) heterofunctionalized monocyclic β-lactams derived from penicillin G
- 1 November 1988
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 23 (6) , 561-571
- https://doi.org/10.1016/0223-5234(88)90100-6
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Penem synthesis through C3-N ring closure of a .beta.-lactam precursorJournal of the American Chemical Society, 1985
- New synthesis of penems via a reductive cyclization reaction of oxalimides with trialkyl phosphite.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- The penems, a new class of .beta.-lactam antibiotics. 2. Total synthesis of racemic 6-unsubstituted representativesJournal of the American Chemical Society, 1979
- The penems, a new class of .beta.-lactam antibiotics: 6-acylaminopenem-3-carboxylic acidsJournal of the American Chemical Society, 1978
- Structure and absolute configuration of thienamycinJournal of the American Chemical Society, 1978
- Hetacillin (R)- and (S)-sulfoxides. Synthesis and structure-activity relationshipsJournal of Medicinal Chemistry, 1978
- 4-Mercapto-2-azetidinone, II1) Darstellung und Reaktionen von 4-Mercapto-2-azetidinonenEuropean Journal of Organic Chemistry, 1974
- Structural studies on penicillin derivatives. IX. Synthesis of thiazolidine-azetidinonesJournal of the American Chemical Society, 1972
- Oxidation of some 1,2-seco-penicillinsJournal of the Chemical Society, Chemical Communications, 1972
- Structural studies on penicillin derivatives. IV. Novel rearrangement of penicillin V sulfoxideJournal of the American Chemical Society, 1970