Substitution of the Participating Group of Glycosyl Donors by a Halogen Atom: Influence on the Rearrangement of Transient Orthoesters Formed during Glycosylation Reactions-Reference-Cited by-同舟云学术

Substitution of the Participating Group of Glycosyl Donors by a Halogen Atom: Influence on the Rearrangement of Transient Orthoesters Formed during Glycosylation Reactions

Published:2017-03-06 Issue:6 Volume:82 Page:3291-3297
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Joosten Antoine¹,Boultadakis-Arapinis Mélissa²,Gandon Vincent³,Micouin Laurent²,Lecourt Thomas¹^ORCID

Affiliation:

1. Normandie Univ, INSA Rouen, UNIROUEN, CNRS, COBRA UMR 6014, 76000 Rouen, France

2. Université Paris Descartes, Sorbonne Paris Cité, CNRS (UMR 8601), 75006 Paris, France

3. Institut de Chimie Moléculaire et des Matériaux d’Orsay, CNRS UMR 8182, Univ. Paris-Sud, Université Paris-Saclay, Bâtiment 420, 91405 Orsay, France

Funder

Agence Nationale de la Recherche

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b03088

Reference35 articles.

1. Twenty Years of Mycobacterial Glycans: Furanosides and Beyond

2. Taming the Reactivity of Glycosyl Iodides To Achieve Stereoselective Glycosidation

3. Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry