Stereoselective synthesis of UDP-2-(2-ketopropyl)galactose aided by di-tert-butylsilylene protecting group.

Abstract:

:UDP-2-(2-ketopropyl)galactose (1) has been utilized as a valuable probe for profiling proteins modified by O-GlcNAc. In this work, we developed a protocol for efficient synthesis of 1. Thus, 2-methallylgalactose derivative 11, a synthetic intermediate for the compound 1, was prepared by stereoselective iodination and methallylation at C-2 position, through exploitation of 4,6-O-di-tert-butylsilylene protecting group.

journal_name

Glycoconj J

journal_title

Glycoconjugate journal

authors

Sakamoto Y,Ohta T,Ito Y

doi

10.1007/s10719-015-9581-y

subject

Has Abstract

pub_date

2015-10-01 00:00:00

pages

541-8

issue

7

eissn

0282-0080

issn

1573-4986

pii

10.1007/s10719-015-9581-y

journal_volume

32

pub_type

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