scispace - formally typeset
C

Coralie Gelis

Researcher at Institut de Chimie des Substances Naturelles

Publications -  8
Citations -  213

Coralie Gelis is an academic researcher from Institut de Chimie des Substances Naturelles. The author has contributed to research in topics: Enantioselective synthesis & Cycloaddition. The author has an hindex of 6, co-authored 8 publications receiving 136 citations. Previous affiliations of Coralie Gelis include Centre national de la recherche scientifique.

Papers
More filters
Journal ArticleDOI

Highly Diastereo- and Enantioselective Synthesis of Cyclohepta[b]indoles by Chiral-Phosphoric-Acid-Catalyzed (4+3) Cycloaddition

TL;DR: The approach described herein provides efficient access to 6-aminotetrahydrocyclohepta[b]indoles in good yields with mostly complete diastereoselectivities and excellent levels of enantioselectivity.
Journal ArticleDOI

Chiral Phosphoric Acid Catalyzed [3 + 2] Cycloaddition and Tandem Oxidative [3 + 2] Cycloaddition: Asymmetric Synthesis of Substituted 3-Aminodihydrobenzofurans.

TL;DR: Asymmetric [3 + 2] cycloaddition of quinones with ene- and thioene-carbamates was achieved by chiral phosphoric acid catalysis, providing the corresponding 3-amino-2,3-dihydrobenzofurans in excellent yields with moderate to good diastereoselectivities and excellent enantioselectivity.
Journal ArticleDOI

Chiral Hypervalent Iodine(III) Catalyst Promotes Highly Enantioselective Sulfonyl- and Phosphoryl-oxylactonizations

TL;DR: An efficient enantioselective hypervalent iodine promoted oxylactonization of 4-pentenoic acids has been achieved using stoichiometric or a catalytic amount of chiral aryl-λ3-iodane.
Journal ArticleDOI

Enantioselective Redox-Divergent Chiral Phosphoric Acid Catalyzed Quinone Diels–Alder Reactions

TL;DR: In this paper, an efficient enantioselective construction of tetrahydronaphthalene-1,4-diones as well as dihydronaphthalene 1,4diols by a chiral phosphoric acid catalyzed quinone Diels-Alder reaction with dienecarbamates is reported.
Journal ArticleDOI

Chiral Phosphoric Acid-Catalyzed Enantioselective Construction of 2,3-Disubstituted Indolines.

TL;DR: In this paper, a wide variety of 2,3-disubstituted 2-aminoindolines, including polycyclic ones, were prepared in generally high yields (up to 98%) with moderate to complete diastereoselectivities and in most cases excellent enanti-lectivities.