HEMI-THIOACETAL PUMMERER REACTION FOR THE SYNTHESIS OF GLIOVIRIN BENZYLIC SULFIDE MODELS

Authors
MAGNUS P MITCHELL IS
Citation
P. Magnus et Is. Mitchell, HEMI-THIOACETAL PUMMERER REACTION FOR THE SYNTHESIS OF GLIOVIRIN BENZYLIC SULFIDE MODELS, Tetrahedron letters, 39(50), 1998, pp. 9131-9134
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
50
Year of publication
1998
Pages
9131 - 9134
Database
ISI
SICI code
0040-4039(1998)39:50<9131:HPRFTS>2.0.ZU;2-0
Abstract
The cyclic hemithioacetal sulfoxide 15 readily undergoes the Pummerer reaction in the presence of carbon nucleophiles to give substituted be nzylic sulfides in excellent yields. (C) 1998 Elsevier Science Ltd. Al l rights reserved.