Solvent Effects in the Nucleophilic Substitutions of Tetrahydropyran Acetals Promoted by Trimethylsilyl Trifluoromethanesulfonate: Trichloroethylene as Solvent for Stereoselective C- and O-Glycosylations-Reference-Cited by-同舟云学术

Solvent Effects in the Nucleophilic Substitutions of Tetrahydropyran Acetals Promoted by Trimethylsilyl Trifluoromethanesulfonate: Trichloroethylene as Solvent for Stereoselective C- and O-Glycosylations

Published:2014-07-03 Issue:14 Volume:16 Page:3684-3687
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kendale Joanna C.¹,Valentín Elizabeth M.¹,Woerpel K. A.¹

Affiliation:

1. Department of Chemistry, New York University, New York, New York 10003, United States

Funder

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol501471c

Reference58 articles.

1. On the reactivity and selectivity of donor glycosides in glycochemistry and glycobiology: trapped covalent intermediates

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3. Mechanism of a Chemical Glycosylation Reaction

4. Thermal effect in β-selective glycosylation reactions using glycosyl iodides

5. A stereospecific route to 2-deoxy-.beta.-glycosides

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