DECONJUGATIVE ALDOL-CYCLIZATION SEQUENCE FOR THE CONSTRUCTION OF SUBSTITUTED 2-METHOXYTETRAHYDROFURANS

Authors
GALATSIS P MANWELL JJ
Citation
P. Galatsis et Jj. Manwell, DECONJUGATIVE ALDOL-CYCLIZATION SEQUENCE FOR THE CONSTRUCTION OF SUBSTITUTED 2-METHOXYTETRAHYDROFURANS, Tetrahedron letters, 36(45), 1995, pp. 8179-8182
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
36
Issue
45
Year of publication
1995
Pages
8179 - 8182
Database
ISI
SICI code
0040-4039(1995)36:45<8179:DASFTC>2.0.ZU;2-3
Abstract
We have shown that the conditions of iodine-pyridine provides a stereo selective method of cyclizing homoallylic alcohols derived from the de conjugative aldol reaction of methyl (E)-4-methoxy-3-butenoate.