New developments in asymmetric Bradsher cycloadditions: use of chiral dienes

Authors
Urban, D Duval, E Langlois, Y
Citation
D. Urban et al., New developments in asymmetric Bradsher cycloadditions: use of chiral dienes, TETRAHEDR L, 41(48), 2000, pp. 9251-9256
Citations number
23
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
48
Year of publication
2000
Pages
9251 - 9256
Database
ISI
SICI code
0040-4039(20001125)41:48<9251:NDIABC>2.0.ZU;2-M
Abstract
Several serinol derivatives have been prepared and condensed following the Zincke reaction with 2,7-naphthyridine. The resulting naphthyridinium salts were engaged in Bradsher cycloadditions with enol ethers and afforded tetr acyclic adducts, potential synthetic precursors of manzamine A alkaloid. (C ) 2000 Elsevier Science Ltd. All rights reserved.