Abstract
Monocyclic cis and trans amino beta-lactams are acetylated with 2-bromo-2-phenylacetyl chloride in aqueous sodium bicarbonate solution. The same reaction with 6-aminopenicillanic acid follows a different pathway and produces an oxazolone.
- Title
- Acetylation of the amino group in beta-lactams under aqueous conditions: Effects of ring sizes
- Creators - without role
- Indrani Banik - Univ Texas MD Anderson Canc Ctr, Dept Mol Pathol, 1515 Holcombe Blvd, Houston, TX 77030 USARam Naresh Yadav - Veer Bahadur Singh Purvanchal UniversityAjay K. Bose - Stevens Institute of TechnologyBimal Krishna Banik - Prince Mohammad bin Fahd University
- Publication Details
- Journal of the Indian Chemical Society, Vol.96(10), pp.1343-1346
- Publisher
- Elsevier
- Number of pages
- 4
- Grant note
- US NCI; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Cancer Institute (NCI) US NIH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA US Kleberg Foundation
- Identifiers
- 9925187708331
- Academic Unit
- Prince Mohammad Bin Fahd University
- Language
- English
- Resource Type
- Journal article