A Diversity-Oriented Strategy for Chemical Synthesis of Glycosphingolipids: Synthesis of Glycosphingolipid LcGg4 and Its Analogues and Derivatives.


Journal

The Journal of organic chemistry
ISSN: 1520-6904
Titre abrégé: J Org Chem
Pays: United States
ID NLM: 2985193R

Informations de publication

Date de publication:
15 01 2021
Historique:
pubmed: 5 1 2021
medline: 5 1 2021
entrez: 4 1 2021
Statut: ppublish

Résumé

A diversity-oriented strategy was developed for the synthesis of glycosphingolipids (GSLs). This strategy was highlighted by using a simple lactoside containing the core structures of GSL glycan and lipid as the universal starting material to obtain different synthetic targets upon stepwise elongation of the glycan via chemical glycosylations and on-site remodeling of the lipid via chemoselective cross-metathesis and

Identifiants

pubmed: 33395290
doi: 10.1021/acs.joc.0c02490
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1633-1648

Auteurs

Rajendra S Rohokale (RS)

Department of Chemistry, University of Florida, 214 Leigh Hall, Gainesville, Florida 32611, United States.

Qingjiang Li (Q)

Department of Chemistry, University of Florida, 214 Leigh Hall, Gainesville, Florida 32611, United States.

Zhongwu Guo (Z)

Department of Chemistry, University of Florida, 214 Leigh Hall, Gainesville, Florida 32611, United States.

Classifications MeSH