Emmanuel Riguet

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 6

Top Topics

Tissue Engineering

Molecular Docking

Top Venues

Chemistry (Weinheim an der Bergstrasse, Germany)

Organic letters

Chemical communications (Cambridge, England)

Organic & biomolecular chemistry

This page only lists publications with an associated author ORCID identifier.

Publications

Morgane Mando, Fabienne Grellepois, Aurélien Blanc, Eric Hénon, Emmanuel Riguet
Toward Efficient and Stereoselective Aromatic and Dearomative Cope Rearrangements: Experimental and Theoretical Investigations of α-Allyl-α'-Aromatic γ-Lactone Derivatives. Chemistry (Weinheim an der Bergstrasse, Germany) 30 (21) (2024)
Morgane Mando, Fabienne Grellepois, Aurélien Blanc, Eric Hénon, Emmanuel Riguet
Toward Efficient and Stereoselective Aromatic and Dearomative Cope Rearrangements: Experimental and Theoretical Investigations of α-Allyl-α'-Aromatic γ-Lactone Derivatives. Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
Morgane Mando, Fabienne Grellepois, Aurélien Blanc, Eric Hénon, Emmanuel Riguet
Toward Efficient and Stereoselective Aromatic and Dearomative Cope Rearrangements: Experimental and Theoretical Investigations of α-Allyl-α'-Aromatic γ-Lactone Derivatives. Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
Morgane Mando, Mathieu Fares, Christelle Kowandy, Fabienne Grellepois, Emmanuel Riguet
Organocatalyzed Asymmetric Allylic Alkylation Enables Synthesis of Chiral γ-Lactones Bearing Vicinal Tertiary and Quaternary Stereocenters. Organic letters 24 (29) (2022)
Gatien Messire, Fabien Massicot, Laura Pascual, Emmanuel Riguet, Jean-Luc Vasse, Jean-Bernard Behr
Broadening the reaction scope of unprotected aldoses via their corresponding nitrones: 1,3-dipolar cycloadditions with alkenes. Organic & biomolecular chemistry 18 (29) (2022)
Morgane Mando, Fabienne Grellepois, Emmanuel Riguet
Organocatalytic enantioselective allylic alkylation of α-aryl γ-lactones: an approach to densely functionalized quaternary stereocentres. Chemical communications (Cambridge, England) 56 (49) (2020)