Synthesis of 2,5-difunctionalised-3,3-dimethylpiperidines via omega-halogenated imines

Authors
Stevens, CV Peristeropoulou, M De Kimpe, N
Citation
Cv. Stevens et al., Synthesis of 2,5-difunctionalised-3,3-dimethylpiperidines via omega-halogenated imines, TETRAHEDRON, 57(37), 2001, pp. 7865-7870
Citations number
19
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
57
Issue
37
Year of publication
2001
Pages
7865 - 7870
Database
ISI
SICI code
0040-4020(20010910)57:37<7865:SO2VO>2.0.ZU;2-B
Abstract
2,5-Difunctionalised-3,3-dimethylpiperidines were prepared by addition of n ucleophiles to piperideinium salts, formed by electrophile-induced cyclisat ion of gamma,delta -unsaturated imines with N-bromosuccinimide in alcoholic medium. (C) 2001 Elsevier Science Ltd. All rights reserved.