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Jean Suffert, Ph.D.

Affiliations: 
Faculté de Pharmacie Université de Strasbourg 
Area:
Organic chemistry, organometallic chemistry, catalysis
Website:
http://www-chimie.u-strasbg.fr/~lsb/
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"Jean Suffert"
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Publications

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Flores O, Locquet P, Suffert J. (2022) An Alternative Route to Complex Allenes or Cyclooctatrienes via a Suzuki Cyclocarbopalladation Cascade. Chemistry (Weinheim An Der Bergstrasse, Germany). 28: e202103502
Flores O, Wagner P, Suffert J. (2021) Cyclocarbopalladation/Stille Cascade: Stereoselective Access to Quaternary Functionalized Carbons. Organic Letters
Salacz L, Girard N, Suffert J, et al. (2019) Synthesis of Aromatic Rings Embedded in Polycyclic Scaffolds by Triyne Cycloaddition: Competition between Carbonylative and Non-Carbonylative Pathways. Molecules (Basel, Switzerland). 24
Salacz L, Girard N, Blond G, et al. (2018) Synthesis of Polyheterocyclic Tropones by [2 + 2 + 2 + 1] Carbonylative Cycloaddition of Triynes. Organic Letters
Salacz L, Girard N, Suffert J, et al. (2018) Carbonylative cycloaddition for the synthesis of medium-sized carbo- and heterocycles Monatshefte FüR Chemie - Chemical Monthly. 149: 671-686
Blouin S, Pertschi R, Schoenfelder A, et al. (2018) Molecular Diversity of Cyclooctatetraenes through Palladium-Catalyzed Cascade Reactions Advanced Synthesis & Catalysis. 360: 2166-2171
Wagner P, Gulea M, Suffert J, et al. (2017) Synthesis of Benzo[c]silole derivatives Bearing a Tetrasubstituted Exocyclic C=C Double Bond by Palladium-Catalyzed Domino Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany)
Salacz L, Charpentier C, Suffert J, et al. (2017) Desymmetrizing Hydroformylation of Dihydromuconic Acid Diesters: Application to the Synthesis of (+/-)-Vindeburnol. The Journal of Organic Chemistry
Suffert J, Blouin S, Blond G, et al. (2017) Cyclocarbopalladation as a Key Step in Cascade Reactions: Recent Developments Synthesis. 49: 1767-1784
Joussot J, Schoenfelder A, Suffert J, et al. (2017) Synthesis of original polycycles containing five-, six- and seven-membered rings through cyclocarbopalladations/C–H activation cascade reactions Comptes Rendus Chimie. 20: 665-681
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