Carbohydrate Research 2012-05-15

Tetraisopropyldisiloxane-1,3-diyl as a versatile protecting group for pentopyranosides.

Richard Johnsson, Richard Johnsson

Index: Carbohydr. Res. 353 , 92-5, (2012)

Full Text: HTML

Abstract

The protecting group tetraisopropyldisiloxane-1,3-yl has been investigated for simultaneous protection of two hydroxyls on pentopyranosides. Methyl α-D-xylopyranoside is protected in excellent regioselectivity and high yield to form the 2,3-protected xylopyranoside whereas methyl β-D-xylopyranoside gives the 3,4-protected product also with excellent regioselectivity.Copyright © 2012 Elsevier Ltd. All rights reserved.


Related Compounds

Related Articles:

Effects of inhibition of proteoglycan synthesis on the differentiation of cultured rat Schwann cells.

1987-08-01

[J. Cell Biol. 105(2) , 1013-21, (1987)]

Transacetylations to carbohydrates catalyzed by acetylxylan esterase in the presence of organic solvent.

2003-10-13

[Biochim. Biophys. Acta 1623 , 62-71, (2003)]

Synthesis of acylated methyl beta-D-xylopyranosides and their enzymic deacylations by rabbit serum esterases.

1997-07-11

[Carbohydr. Res. 302(1-2) , 13-8, (1997)]

Determination of sugar structures in solution from residual dipolar coupling constants: methodology and application to methyl beta-D-xylopyranoside.

2004-10-13

[J. Am. Chem. Soc. 126(40) , 13100-10, (2004)]

Mode of action of acetylxylan esterase from Streptomyces lividans: a study with deoxy and deoxy-fluoro analogues of acetylated methyl beta-D-xylopyranoside.

2003-07-23

[Biochim. Biophys. Acta 1622(2) , 82-8, (2003)]

More Articles...