New phenylselanyl group activation: synthesis of aziridines and oxazolidin-2-onesElectronic Supplementary Information (ESI) available: experimental section. See http://www.rsc.org/suppdata/ob/b4/b406566m/
- 11 May 2004
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 2 (11) , 1575-1576
Abstract
After the study of different phenylselanyl group activators, halogenation by N-bromosuccinimide (NBS) has been shown to be the most suitable manner for cyclizing β-phenylselanyl amines into aziridines and also enabled production of oxazolidin-2-ones from N-Boc β-phenylselanyl amines in excellent yield.Keywords
This publication has 1 reference indexed in Scilit:
- Inter and Intramolecular Nucleophilic Substitutions of Activated Phenylselanyl GroupsPhosphorus, Sulfur, and Silicon and the Related Elements, 2001