» Articles » PMID: 18491016

Conformationally Armed Glycosyl Donors: Reactivity Quantification, New Donors and One Pot Reactions

Overview
Specialty Chemistry
Date 2008 May 21
PMID 18491016
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

The relative reactivity of conformationally armed thioglycosides is quantified.

Citing Articles

Expedient Synthesis of Superarmed Glycosyl Donors via Oxidative Thioglycosidation of Glycals.

Forsythe N, Mize E, Kashiwagi G, Demchenko A Synthesis (Stuttg). 2024; 56(7):1147-1156.

PMID: 38655286 PMC: 11034933. DOI: 10.1055/a-2183-0175.


Synthesis and Glycosidation of Anomeric Halides: Evolution from Early Studies to Modern Methods of the 21st Century.

Singh Y, Geringer S, Demchenko A Chem Rev. 2022; 122(13):11701-11758.

PMID: 35675037 PMC: 9417321. DOI: 10.1021/acs.chemrev.2c00029.


GH47 and Other Glycoside Hydrolases Catalyze Glycosidic Bond Cleavage with the Assistance of Substrate Super-arming at the Transition State.

Quirke J, Crich D ACS Catal. 2021; 11:10308-10315.

PMID: 34777906 PMC: 8579916. DOI: 10.1021/acscatal.1c02750.


Bromine-Promoted Glycosidation of Conformationally Superarmed Thioglycosides.

Panza M, Civera M, Yasomanee J, Belvisi L, Demchenko A Chemistry. 2019; 25(51):11831-11836.

PMID: 31286579 PMC: 6742554. DOI: 10.1002/chem.201901969.


Furanosyl Oxocarbenium Ion Conformational Energy Landscape Maps as a Tool to Study the Glycosylation Stereoselectivity of 2-Azidofuranoses, 2-Fluorofuranoses and Methyl Furanosyl Uronates.

van der Vorm S, Hansen T, van Rijssel E, Dekkers R, Madern J, Overkleeft H Chemistry. 2019; 25(29):7149-7157.

PMID: 30882938 PMC: 6563709. DOI: 10.1002/chem.201900651.