| Literature DB >> 17962745 |
Aliasghar Jarrahpour1, Maaroof Zarei.
Abstract
New cis monocyclic beta-lactams were synthesized by [2+2] Staudinger cycloaddition reactions of the imine (3,4-dimethoxybenzylidene)-(4-methoxyphenyl)-amine and ketenes derived from different acyl chlorides and Et3N. These monocyclic beta-lactams were then cleaved by ceric ammonium nitrate (CAN) to give NH-monocyclic beta-lactams, which in turn were converted to N-sulfonyl monocyclic beta-lactams by treatment with four different sulfonyl chlorides in the presence of Et3N and 4,4-dimethyl-aminopyridine (DMAP).Entities:
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Year: 2006 PMID: 17962745 PMCID: PMC6148652 DOI: 10.3390/11010049
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411