Total Synthesis of a Chimeric Glycolipid Bearing the Partially Acetylated Backbone of Sponge-Derived Agminoside E-Reference-Cited by-同舟云学术

Total Synthesis of a Chimeric Glycolipid Bearing the Partially Acetylated Backbone of Sponge-Derived Agminoside E

Published:2021-10-21 Issue:21 Volume:86 Page:15357-15375
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Muru Kevin¹,Cloutier Maude¹,Provost-Savard Arianne¹,Di Cintio Sabrina¹,Burton Océane¹,Cordeil Justin¹,Groleau Marie-Christine¹,Legault Jean²,Déziel Eric¹,Gauthier Charles¹^ORCID

Affiliation:

1. Centre Armand-Frappier Santé Biotechnologie, Institut National de la Recherche Scientifique (INRS), 531, boulevard des Prairies, Laval, Québec H7V 1B7, Canada

2. Département des Sciences Fondamentales, Université du Québec à Chicoutimi (UQAC), 555, boulevard de l’Université, Chicoutimi, Québec G7H 2B1, Canada

Funder

Fonds de Recherche du Qu??bec - Sant??

Fonds de Recherche du Qu??bec - Nature et Technologies

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01907

Reference64 articles.

1. Glycolipids of Marine Invertebrates

2. Chemistry and Biology of Bioactive Glycolipids of Marine Origin

3. The Agminosides: Naturally Acetylated Glycolipids from the New Zealand Marine Sponge Raspailia agminata

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. C7 Epimerization of Benzylidene-Protected β-D-Idopyranosides Brings Structural Insights into Idose Conformational Flexibility;J ORG CHEM;2022

2. C7 Epimerization of Benzylidene-Protected β-d-Idopyranosides Brings Structural Insights into Idose Conformational Flexibility;The Journal of Organic Chemistry;2022-09-22