Carbohydrate Research 2002-10-11

A mild and selective method for cleavage of O-acetyl groups with dibutyltin oxide.

Hong-Min Liu, Xuebin Yan, Wen Li, Conghai Huang

Index: Carbohydr. Res. 337(19) , 1763-7, (2002)

Full Text: HTML

Abstract

A mild and efficient neutral method for the cleavage of O-acetyl groups with dibutyltin oxide has been developed. This method is especially useful in the synthesis of glycosides containing base- or acid-sensitive multifunctional groups.


Related Compounds

Related Articles:

Copolyesters made from 1,4-butanediol, sebacic acid, and D-glucose by melt and enzymatic polycondensation.

2015-03-09

[Biomacromolecules 16(3) , 868-79, (2015)]

Hydrogen-bond-mediated self-assembly of 26-membered diaza tetraester crowns of 3,5-disubstituted 1H-pyrazole. Dimerization study in the solid state and in CDCl3 solution.

2011-10-21

[J. Org. Chem. 76(20) , 8223-31, (2011)]

Dibutyltin oxide--phenyl isocyanate system for regioselective phenylcarbamoylation of the hydroxy-groups of ribonucleosides.

1980-01-01

[Nucleic Acids Symp. Ser. (8) , s7-8, (1980)]

[Preparation and spectroscopic studies of diorganotin(IV) complexes with adenosine and related compounds].

2000-01-01

[Acta Pharm. Hung. 70(3-6) , 119-30, (2000)]

Synthesis of 2- and 4-nitrophenyl beta-glycosides of beta-(1-->4)- D-xylo-oligosaccharides of dp 2-4.

1995-11-22

[Carbohydr. Res. 277(2) , 231-44, (1995)]

More Articles...