The ring closure of substituted azetidinones: a new route to [4.2.0] fused beta-lactams

Autor:	C. L. Jordan, Robert J. Ternansky
Rok vydání:	1993
Předmět:	Organic Chemistry Clinical Biochemistry Closure (topology) Pharmaceutical Science Ring (chemistry) Biochemistry Combinatorial chemistry Beta-lactam chemistry.chemical_compound chemistry Intramolecular force Drug Discovery Molecular Medicine Molecular Biology Derivative (chemistry)
Zdroj:	Bioorganic & Medicinal Chemistry Letters. 3:2443-2446
ISSN:	0960-894X
Popis:	The synthesis of 1-carba-1-dethiacephalosporin nuclei is described. The new route utilizes a readily-available penicillin derivative as starting material and features an intramolecular ring closure to form the six-membered ring.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::1a5e0841c985598d46fbbfc91c460a52 https://doi.org/10.1016/s0960-894x(01)80974-4 Zobrazit plný text záznamu