Stereoselective radical addition of tertiary amines to (5R)-5-menthyloxy-2[5H]-furanone: Application to the enantioselective synthesis of (-)-isoretronecanol and (+)-laburnine

Authors
Bertrand, S Hoffmann, N Pete, JP
Citation
S. Bertrand et al., Stereoselective radical addition of tertiary amines to (5R)-5-menthyloxy-2[5H]-furanone: Application to the enantioselective synthesis of (-)-isoretronecanol and (+)-laburnine, TETRAHEDR L, 40(16), 1999, pp. 3173-3174
Citations number
9
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
16
Year of publication
1999
Pages
3173 - 3174
Database
ISI
SICI code
0040-4039(19990416)40:16<3173:SRAOTA>2.0.ZU;2-Q
Abstract
The adducts of a stereoselective radical addition of tertiary amines with ( 5R)-5-menthyloxy-2[5H]-furanone were transformed very efficiently into enan tiomerically pure pyrrolizidine and indolizidine alkaloids. through a three steps sequence. (C) 1999 Published by Elsevier Science Ltd. All rights res erved.