D. Pardo

发表

Enantioselective ring expansion of prolinol derivatives. Two formal syntheses of (−)-swainsonine

J. Cossy, D. G. Pardo, I. Déchamps, 2007 .

Ring Expansion Induced by DAST: Synthesis of Substituted 3-Fluoropiperidines from Prolinols and 3-Fluoroazepanes from 2-Hydroxymethylpiperidines

J. Cossy, D. G. Pardo, I. Déchamps, 2007 .

Highly Enantioselective Synthesis of β-Amino Alcohols

J. Cossy, D. G. Pardo, J. Appenzeller, 2006 .

Rearrangement of beta-amino alcohols and application to the synthesis of biologically active compounds.

O. Mirguet, J. Cossy, D. G. Pardo, 2009, Chirality.

Enantioselective diethylzinc addition to aromatic and aliphatic aldehydes using (3R,5R)-dihydroxypiperidine derivatives catalyst

J. Cossy, D. G. Pardo, Rémi Roudeau, 2006 .

Ring expansion: formal total synthesis of (−)-paroxetine

O. Mirguet, J. Desmurs, J. Cossy, 2001 .

Synthesis of Two Neurokinin NK1 Receptor Antagonists: (+)-L-733,060 and (-)-L-733,061

J. Cossy, D. G. Pardo, Anne Cochi, 2012 .

Ring Expansion: Synthesis of the Velbanamine Piperidine Core

O. Mirguet, J. Cossy, D. G. Pardo, 2002 .

A SHORT AND EFFICIENT SYNTHESIS OF ZAMIFENACIN A MUSCARINIC M3 RECEPTOR ANTAGONIST

J. Cossy, D. G. Pardo, C. Dumas, 1997 .

Diastereoselective conjugate addition of organocuprates to chiral racemic olefinic amido esters. Formal total synthesis of paroxetine

O. Mirguet, J. Desmurs, J. Cossy, 2003 .

A new nitrone from C2 symmetric piperidine for the synthesis of hydroxylated indolizidinone

S. Cicchi, A. Brandi, J. Cossy, 2002 .

Ring Expansion: Formal Total Synthesis of (‐)‐Paroxetine.

O. Mirguet, J. Desmurs, J. Cossy, 2002 .

A short formal synthesis of paroxetine. Diastereoselective cuprate addition to a chiral racemic olefinic amido ester

O. Mirguet, J. Desmurs, J. Cossy, 2001 .

Ring Expansion – Formation of Optically Active 3-Hydroxypiperidines from Pyrrolidinemethanol Derivatives

J. Cossy, D. G. Pardo, C. Dumas, 1999 .

Formation of optically active 3-hydroxypiperidines

J. Cossy, D. G. Pardo, P. Michel, 1995 .

A very useful and mild method for the protection and deprotection of carboxylic acids

M. Scheloske, J. Cossy, D. G. Pardo, 1994 .

Synthesis of Substituted α-Trifluoromethyl Piperidinic Derivatives

J. Cossy, D. G. Pardo, Sarah Rioton, 2017, Molecules.

Access to Optically Active 3‐Aminopiperidines by Ring Expansion of Prolinols: Thermodynamic versus Kinetic Control

J. Cossy, D. G. Pardo, Anne Cochi, 2012 .

Access to optically active 3-azido- and 3-aminopiperidine derivatives by enantioselective ring expansion of prolinols.

J. Cossy, D. G. Pardo, Anne Cochi, 2011, Organic letters.

Enantioselective Ring Expansionof Prolinols: An Efficient and Short Synthesis of 2-Phenylpiperidin-3-olDerivatives and 3-Hydroxypipecolic Acids

J. Cossy, Yang Zhao, C. Navarro, 2009 .

Palladium-Catalyzed Intermolecular α-Arylation of N-Protected 2-Piperidinones.

J. Cossy, and Arnault de Filippis, D. Pardo, 2003 .

Palladium-Catalyzed Intermolecular α-Arylation of N-Protected 2-Piperidinones

J. Cossy, D. G. Pardo, and Arnault de Filippis, 2003 .

Rearrangement of N-alkyl 1,2-amino alcohols. Synthesis of (S)-toliprolol and (S)-propanolol

J. Cossy, D. G. Pardo, T. Métro, 2009 .

Highly enantioselective synthesis of beta-amino alcohols.

J. Cossy, D. G. Pardo, J. Appenzeller, 2006, Organic letters.

Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of beta-amino alcohols.

J. Cossy, D. G. Pardo, T. Métro, 2008, The Journal of organic chemistry.

Enantioselective synthesis and physicochemical properties of libraries of 3-amino- and 3-amidofluoropiperidines.

Wolfgang H. B. Sauer, J. Cossy, Agnès Bombrun, 2014, Chemistry.

Ring enlargement and ring contraction induced by DAST

D. G. Pardo, L. Hijfte, A. Cossy, 2010 .

Monoalkylation of acetonitrile by primary alcohols catalyzed by iridium complexes.

J. Cossy, D. G. Pardo, Gino Ricci, 2011, Organic letters.

Synthesis of Functionalized 4‐Fluoropyridazines

J. Cossy, D. G. Pardo, Pavel K. Mykhailiuk, 2017 .

Synthesis of α‐(Trifluoromethyl)pyridazine Derivatives

J. Cossy, D. G. Pardo, Alexandra Feraldi‐Xypolia, 2018 .

Daucus carota mediated-reduction of cyclic 3-oxo-amines.

J. Cossy, D. G. Pardo, Romain Lacheretz, 2009, Organic letters.

The thermal rearrangement of N-alkyl-N-vinylpropargylamines into 2-methylpyrroles. A new synthesis of annulated[b]pyrroles

J. Cossy, D. G. Pardo, C. Poitevin, 1996 .

Highly enantioselective synthesis of beta-amino alcohols: a catalytic version.

J. Cossy, D. G. Pardo, T. Métro, 2007, The Journal of organic chemistry.

The iodocyclization of unsaturated dihydroxysulfonamide derivatives. N- versus O-cyclization

J. Cossy, D. G. Pardo, D. Belotti, 2001 .