๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A Glycosidation Reaction Employing Montmorillonite K-10 as Catalyst

โœ Scribed by Bedell, Brooke L.; Crouch, R. David; Holden, Michael S.; Martinson, Heidi E.


Book ID
121088646
Publisher
American Chemical Society
Year
1996
Tongue
English
Weight
42 KB
Volume
73
Category
Article
ISSN
0021-9584

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Novel stereocontrolled glycosidations of
โœ Takaaki Jyojima; Naoki Miyamoto; Yasumasa Ogawa; Shuichi Matsumura; Kazunobu Tos ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 234 KB

Novel stereocontrolled glycosidations of 3,4-di-O-wotected olivoses and alcohols using a heterogenem~ and environmentally benign solid acid, montmoriilonite K-10, have been developed. The glycosidatlons of the 3-O-Ac-4-O-TBS-olivuse (4) and various alcohols using montmorilionite K-10 in CH2CI2 at 25

ChemInform Abstract: Montmorillonite K-1
โœ A.-X. LI; T.-S. LI; T.-H. DING ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 29 KB

Montmorillonite K-10 and KSF as Remarkable Acetylation Catalysts. -The title compounds are good catalysts for the acetylation of compounds such as (I), (IV), and (VI) but not for tertiary alcohols. The method presented has the additional advantages of mild conditions, high yield, easy separation an