Exclusive 1,4-aryl migration in a stereoselective cyclization of N-benzylalk-4-enylaminyl radicals

Authors
Senboku, H Hasegawa, H Orito, K Tokuda, M
Citation
H. Senboku et al., Exclusive 1,4-aryl migration in a stereoselective cyclization of N-benzylalk-4-enylaminyl radicals, TETRAHEDR L, 41(30), 2000, pp. 5699-5703
Citations number
29
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
30
Year of publication
2000
Pages
5699 - 5703
Database
ISI
SICI code
0040-4039(20000722)41:30<5699:E1MIAS>2.0.ZU;2-Y
Abstract
Tandem cyclization of N-benzylalk-4-enylaminyl radicals readily occurs to g ive 1,4-aryl migration pyrrolidines, trans-N-methyl-2-alkyl-5-(1-phenylalky l)pyrrolidines, exclusively. (C) 2000 Elsevier Science Ltd. All rights rese rved.