2,3-Di-O-picolinyl building blocks as glycosyl donors with switchable stereoselectivity
Author:
Affiliation:
1. Department of Chemistry and Biochemistry
2. University of Missouri – St. Louis
3. One University Boulevard
4. St. Louis
5. USA
Abstract
Coordination of 2,3-di-O-picolinyl protected glycosyl donors with PdBr2 allows to “switch” the stereoselectivity of glycosylations from β- to α-.
Funder
Division of Chemistry
Mizutani Foundation for Glycoscience
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB00107F
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1. Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry
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