S. Reymond

发表

Formal chemoselective synthesis of leucascandrolide A.

P. Capdevielle, J. Cossy, L. Ferrié, 2007, Organic letters.

Neopeltolide, a new promising antitumoral agent

J. Cossy, S. Reymond, J. Gallon, 2008 .

Synthetic Studies toward the C14-C29 Fragment of Mirabalin.

P. Phansavath, V. Ratovelomanana-Vidal, J. Cossy, 2016, Organic letters.

Lewis Acid Catalyzed Synthesis of Cyclic Carbonates, Precursors of 1,2‐ and 1,3‐Diols

J. Cossy, S. Reymond, A. Guérinot, 2014 .

Formal synthesis of dictyostatin and synthesis of two dictyostatin analogues.

J. Cossy, S. Reymond, J. Gallon, 2012, Chemistry.

Synthetic efforts toward the macrolactone core of Leucascandrolide A.

P. Capdevielle, J. Cossy, L. Ferrié, 2008, The Journal of organic chemistry.

Formal Chemoselective Synthesis of Leucascandrolide A.

P. Capdevielle, J. Cossy, L. Ferrié, 2007 .

Copper-catalysed amidation of 2-chloro-pyridines

I. Stansfield, L. Meerpoel, J. Cossy, 2013 .

Synthesis of complex oxygenated heterocycles

A. Corbu, J. Cossy, S. Reymond, 2013 .

Copper-catalyzed Diels-Alder reactions.

J. Cossy, S. Reymond, 2008, Chemical reviews.

Triphenylphosphine: a catalyst for the synthesis of C-aryl furanosides from furanosyl halides

I. Stansfield, L. Meerpoel, J. Cossy, 2014 .

Cobalt-catalyzed diastereoselective synthesis of C-furanosides. Total synthesis of (-)-isoaltholactone.

I. Stansfield, L. Meerpoel, J. Cossy, 2013, The Journal of organic chemistry.

Migrastatin and analogues: New anti-metastatic agents

J. Cossy, S. Reymond, 2008 .

Synthesis of migrastatin and its macrolide core

J. Cossy, S. Reymond, 2007 .

Total Synthesis of (+)‐Migrastatin

J. Cossy, S. Reymond, 2006 .

Synthetic strategy toward the C44-C65 fragment of mirabalin.

P. Phansavath, V. Ratovelomanana-Vidal, J. Cossy, 2014, Organic letters.

Isolation, structural determination and synthetic approaches toward amphidinol 3.

J. Cossy, G. Hanquet, S. Reymond, 2014, Natural product reports.

Iron-catalyzed cross-coupling between C-bromo mannopyranoside derivatives and a vinyl Grignard reagent: toward the synthesis of the C31–C52 fragment of amphidinol 3

J. Cossy, G. Hanquet, S. Reymond, 2013 .

Iron-catalyzed cross-coupling of alkyl halides with alkenyl grignard reagents.

J. Cossy, S. Reymond, A. Guérinot, 2007, Angewandte Chemie.

Iron- and cobalt-catalyzed arylation of azetidines, pyrrolidines, and piperidines with Grignard reagents.

Janine Cossy, J. Cossy, Paola Ciapetti, 2014, Organic letters.

Total synthesis of dolastatin 10 through ruthenium-catalyzed asymmetric hydrogenations

V. Ratovelomanana-Vidal, B. B. Hassine, J. Genêt, 2007 .

Lewis basicity modulation of N-heterocycles: a key for successful cross-metathesis.

J. Cossy, S. Reymond, A. Guérinot, 2014, Organic letters.

Iron- and indium-catalyzed reactions toward nitrogen- and oxygen-containing saturated heterocycles.

J. Cossy, Anna Serra-Muns, S. Reymond, 2015, Accounts of chemical research.

FeCl3·6H2O, a catalyst for the diastereoselective synthesis of cis-isoxazolidines from N-protected δ-hydroxylamino allylic acetates.

J. Cossy, S. Reymond, A. Guérinot, 2013, The Journal of organic chemistry.

Ritter Reaction: Recent Catalytic Developments

J. Cossy, S. Reymond, A. Guérinot, 2012 .

FeCl3-catalyzed Ritter reaction. Synthesis of amides

J. Cossy, S. Reymond, A. Guérinot, 2009 .

Synthesis of both syn and anti diastereoisomers of Boc-dolaproine from (S)-proline through DKR using ruthenium-catalyzed hydrogenation: a dramatic role of N-protecting groups

V. Ratovelomanana-Vidal, J. Genêt, S. Reymond, 2004 .

FeCl(3)-Catalyzed highly diastereoselective synthesis of substituted piperidines and tetrahydropyrans.

J. Cossy, Anna Serra-Muns, S. Reymond, 2010, Organic letters.

FeCl3·6H2O-catalyzed synthesis of substituted cis-2,6-tetrahydropyrans from ζ-hydroxy allylic derivatives

J. Cossy, Anna Serra-Muns, S. Reymond, 2011 .

Silica gel-mediated rearrangement of allylic acetates. Application to the synthesis of 1,3-enynes.

J. Cossy, Anna Serra-Muns, S. Reymond, 2010, Chemical communications.

Diastereoselective synthesis of the C14–C29 fragment of amphidinol.

J. Cossy, G. Hanquet, S. Reymond, 2013, Organic & biomolecular chemistry.

Diastereoselective synthesis of the C17-C30 fragment of amphidinol 3.

D. Hazelard, J. Cossy, T. Kreuzer, 2012, Organic & biomolecular chemistry.

First Iminodiazaphospholidines with a Stereogenic Phosphorus Center. Application to Asymmetric Copper-Catalyzed Cyclopropanation

J. Brunel, S. Reymond, G. Buono, 1999 .

First Iminodiazaphospholidines with a Stereogenic Phosphorus Center. Application to Asymmetric Copper-Catalyzed Cyclopropanation.

J. Brunel, S. Reymond, G. Buono, 1999 .

Ritter Reaction: Recent Catalytic Developments

J. Cossy, S. Reymond, A. Guérinot, 2012 .

FeCl3‐Catalyzed Ritter Reaction. Synthesis of Amides.

J. Cossy, S. Reymond, A. Guérinot, 2009 .

Diastereoselective Metal-Catalyzed Synthesis ofC-Aryl andC-Vinyl Glycosides

P. Bonnet, I. Stansfield, L. Meerpoel, 2012 .

Diastereoselective metal-catalyzed synthesis of C-aryl and C-vinyl glycosides.

P. Bonnet, I. Stansfield, L. Meerpoel, 2012, Angewandte Chemie.

New chiral organophosphorus derivatizing agent for the determination of enantiomeric composition of chloro- and bromohydrins by 31P NMR spectroscopy

J. Brunel, S. Reymond, G. Buono, 2000 .

Total synthesis of (-)-spongidepsin.

P. Capdevielle, J. Cossy, L. Ferrié, 2006, Organic letters.

Triphenylphosphine: A Catalyst for the Synthesis of C‐Aryl Furanosides from Furanosyl Halides.

I. Stansfield, L. Meerpoel, J. Cossy, 2014 .

Chemoselective reactions: Toward the synthesis of biologically active natural products with anticancer activities

P. Capdevielle, J. Cossy, L. Ferrié, 2008 .

Chemoselective cross-metathesis reaction between electron-deficient 1,3-dienes and olefins

P. Capdevielle, J. Cossy, V. Bellosta, 2006 .

Letter to the editor regarding: “New development in the enantioselective ring opening of meso-epoxides by various chloride ion silicon sources catalyzed by an o-methoxyaryldiazaphosphonamide Lewis base”

J. Brunel, S. Reymond, G. Buono*, 2002 .

New development in the enantioselective ring opening of meso-epoxides by various chloride ion silicon sources catalyzed by an o-methoxyaryldiazaphosphonamide Lewis base

J. Brunel, S. Reymond, G. Buono*, 2000 .

Chiral o‐Methoxyaryldiazaphosphonamides − A New Class of Efficient Lewis Bases in the Catalytic Asymmetric Ring Opening of Cyclooctene Oxide with Silicon Tetrachloride

J. Brunel, S. Reymond, O. Legrand, 2002 .

Iron‐ and Indium‐Catalyzed Reactions Toward Nitrogen‐ and Oxygen‐Containing Saturated Heterocycles

J. Cossy, Anna Serra-Muns, S. Reymond, 2015 .

Convergent Synthesis of the C18-C30 Fragment of Amphidinol 3

J. Cossy, T. Kreuzer, S. Reymond, 2009 .

Stereoselective synthesis of the C(53)-C(67) polyene fragment of amphidinol 3

J. Cossy, T. Kreuzer, L. Ferrié, 2007 .