Plausible Transition States for glycosylation reactions

Whitfield, DM

HERO ID

1444729

Reference Type

Journal Article

Year

2012

Language

English

PMID

22525097

HERO ID 1444729
In Press No
Year 2012
Title Plausible Transition States for glycosylation reactions
Authors Whitfield, DM
Journal Carbohydrate Research
Volume 356
Page Numbers 180-190
Abstract The Transition State (TS) for any chemical glycosylation reaction is not known with certainty. Both experimental and computational approaches have been limited due to the complexity of the problem. This work describes a preliminary computational ionization approach using density functional theory calculations to arrive at hypothetical TSs. The new TSs contain the glycosyl donor as anomeric triflates, the acceptor as methanol, some CH(2)Cl(2) molecules, and a Li(+) ion promoter. In this computational approach all glycosylations are disassociative in that the C-1-O(Tf) bond length is greater then 2 Å before any nucleophilic attack. All nucleophilic attack requires some preassociation of the nucleophile with examples of the pre-attack complexation to donor oxygens. These hypothetical models are intended to guide both experimental and computational approaches to finding TSs for glycosylation reactions that can be used to optimize stereoselectivity of glycosylation.
Doi 10.1016/j.carres.2012.03.040
Pmid 22525097
Wosid WOS:000305338000018
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science WOS:000305338000018
Is Public Yes
Language Text English
Keyword Glycosylation; Transition states; Density functional theory; Oxacarbenium ion