| Literature DB >> 15056969 |
Kazuhito Hioki1, Hiroko Kobayashi, Rumi Ohkihara, Shohei Tani, Munetaka Kunishima.
Abstract
Weinreb amides were successfully prepared from the corresponding carboxylic acids using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) in the solvents, methanol, isopropyl alcohol, and acetonitrile, which can solubilize DMT-MM. A variety of carboxylic acids were converted to the corresponding Weinreb amides in excellent yields by simply mixing with DMT-MM and N,O-dimethylhydroxylamine hydrochloride.Entities:
Mesh:
Substances:
Year: 2004 PMID: 15056969 DOI: 10.1248/cpb.52.470
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645