Publications by authors named "Jean Suffert"

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An Alternative Route to Complex Allenes or Cyclooctatrienes via a Suzuki Cyclocarbopalladation Cascade.
Océane Flores, Pierre Locquet, Jean Suffert

Chemistry· January 2022

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Cyclocarbopalladation/Stille Cascade: Stereoselective Access to Quaternary Functionalized Carbons.
Océane Flores, Patrick Wagner, Jean Suffert

Org Lett· August 2021

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Synthesis of Aromatic Rings Embedded in Polycyclic Scaffolds by Triyne Cycloaddition: Competition between Carbonylative and Non-Carbonylative Pathways.
Laura Salacz, Nicolas Girard, Jean Suffert, Gaëlle Blond

Molecules· February 2019

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Synthesis of Polyheterocyclic Tropones by [2 + 2 + 2 + 1] Carbonylative Cycloaddition of Triynes.
Laura Salacz, Nicolas Girard, Gaëlle Blond, Jean Suffert

Org Lett· July 2018

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Synthesis of Benzo[c]silole Derivatives Bearing a Tetrasubstituted Exocyclic C=C Double Bond by Palladium-Catalyzed Domino Reactions.
Patrick Wagner, Mihaela Gulea, Jean Suffert, Morgan Donnard

Chemistry· June 2017

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Desymmetrizing Hydroformylation of Dihydromuconic Acid Diesters: Application to the Synthesis of (±)-Vindeburnol.
Laura Salacz, Cyrille Charpentier, Jean Suffert, Nicolas Girard

J Org Chem· February 2017

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Synthesis of Cyclooctatetraenes through a Palladium-Catalyzed Cascade Reaction.
Sarah Blouin, Vincent Gandon, Gaëlle Blond, Jean Suffert

Angew Chem Int Ed Engl· June 2016

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Aerobic Copper-Mediated Domino Three-Component Approach to 2-Aminobenzothiazole Derivatives.
Thomas Castanheiro, Jean Suffert, Mihaela Gulea, Morgan Donnard

Org Lett· June 2016

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Recent advances in the chemistry of organic thiocyanates.
Thomas Castanheiro, Jean Suffert, Morgan Donnard, Mihaela Gulea

Chem Soc Rev· February 2016

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Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process.
Pierre Regenass, Jean-François Margathe, André Mann, Jean Suffert, Marcel Hibert

Chem Commun (Camb)· September 2014

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Cyclocarbopalladation/cross-coupling cascade reactions in sulfide series: access to sulfur heterocycles.
Thomas Castanheiro, Morgan Donnard, Mihaela Gulea, Jean Suffert

Org Lett· June 2014

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Fenestranes in synthesis: unique and highly inspiring scaffolds.
Aicha Boudhar, Mélanie Charpenay, Gaëlle Blond, Jean Suffert

Angew Chem Int Ed Engl· December 2013

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An expeditious and atom-economical synthesis of a new generation of substituted [4.6.4.6]fenestradienes.
Mélanie Charpenay, Aïcha Boudhar, Gaëlle Blond, Jean Suffert

Angew Chem Int Ed Engl· April 2012

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Step-economical synthesis of taxol-like tricycles through a palladium-catalyzed domino reaction.
Julien Petrignet, Aicha Boudhar, Gaëlle Blond, Jean Suffert

Angew Chem Int Ed Engl· March 2011

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Synthesis of exotic polycycles such as cyclooctatrienes and fenestrenes with differential pro-apoptotic activities on human TRAIL-resistant metastatic cell lines.
Catherine Hulot, Jean Peluso, Gaëlle Blond, Christian D Muller, Jean Suffert

Bioorg Med Chem Lett· November 2010

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Understanding the torquoselectivity in 8pi-electrocyclic cascade reactions: synthesis of fenestradienes versus cyclooctatrienes.
Catherine Hulot, Shadi Amiri, Gaëlle Blond, Peter R Schreiner, Jean Suffert

J Am Chem Soc· September 2009

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Synthesis of [4.6.4.6]fenestradienes and [4.6.4.6]fenestrenes based on an 8pi-6pi-cyclization-oxidation cascade.
Catherine Hulot, Gaëlle Blond, Jean Suffert

J Am Chem Soc· April 2008

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A new pd-catalyzed cascade reaction for the synthesis of strained aromatic polycycles.
Gaëlle Blond, Christophe Bour, Bahaâ Salem, Jean Suffert

Org Lett· March 2008

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Cyclocarbopalladation involving an unusual 1,5-palladium vinyl to aryl shift as termination step: theoretical study of the mechanism.
Antonio J Mota, Alain Dedieu, Christophe Bour, Jean Suffert

J Am Chem Soc· May 2005

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Cyclocarbopalladation: sequential cyclization and C-h activation/Stille cross-coupling in the Pd-5-exo-dig reaction.
Christophe Bour, Jean Suffert

Org Lett· February 2005

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A 4-exo-dig cyclocarbopalladation/8pi electrocyclization cascade: expeditious access to the tricyclic core structures of the ophiobolins and aleurodiscal.
Bahaâ Salem, Jean Suffert

Angew Chem Int Ed Engl· May 2004

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Cyclocarbopalladation: 5-exo-dig cyclization versus direct Stille cross-coupling reaction. The influence of the alpha,beta-propargylic substitution.
Bahaâ Salem, Estelle Delort, Philippe Klotz, Jean Suffert

Org Lett· June 2003

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Cyclocarbopalladation: formation of bicyclic 1,2-cyclobutanediols through a rare 4-exo-dig cyclization.
Bahaâ Salem, Philippe Klotz, Jean Suffert

Org Lett· March 2003

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Cascade cyclization: an easy access to highly unsaturated polycyclic ring systems through a tandem stille/[4 + 2] reaction under mild conditions.
Sébastien Brückner, Estelle Abraham, Philippe Klotz, Jean Suffert

Org Lett· October 2002

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General Method for the Preparation of Alkyne-Functionalized Oligopyridine Building Blocks.
Raymond Ziessel, Jean Suffert, Marie-Thérèse Youinou

J Org Chem· September 1996

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