ACYLOIN REARRANGEMENT OF ALPHA-HYDROXY ACETALS - APPLICATION TO THE METHYL L-MYCAROSIDE SYNTHESIS

Authors
SATO T NAGATA T MAEDA K OHTSUKA S
Citation
T. Sato et al., ACYLOIN REARRANGEMENT OF ALPHA-HYDROXY ACETALS - APPLICATION TO THE METHYL L-MYCAROSIDE SYNTHESIS, Tetrahedron letters, 35(28), 1994, pp. 5027-5030
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
28
Year of publication
1994
Pages
5027 - 5030
Database
ISI
SICI code
0040-4039(1994)35:28<5027:AROAA->2.0.ZU;2-J
Abstract
Acid treatment of alpha-hydroxy acetals induced 1,2-alkyl, aryl, or al kenyl migration. An alkenyl migration product was utilized as a starti ng material of methyl L-mycaroside synthesis.