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The 356 publications of STeRéO

Format: 2022
Reference Graphical abstract HAL

Synthetic Studies on the MARDi Cascade: Stereoselective Preparation of Sulfonyl-Substituted Seven-Membered Rings

Yoann Coquerel, David Bensa, Vincent Moret, Jean Rodriguez, SYNLETT, 2006, 2006, 2751-2754. <hal-02989815>

Synthetic Studies on the MARDi Cascade: Stereoselective Synthesis of Heterocyclic Seven-Membered Rings

Yoann Coquerel, David Bensa, Alain Doutheau, Jean Rodriguez, Organic Letters, 2006, 8, 4819-4822. <hal-02989798>

Unique Michael Addition-Initiated Domino Reaction for the Stereoselective Synthesis of Functionalized Macrolactones from r-Nitroketones in Water

Giorgio Giorgi, Sonia Miranda, Pilar Lopez-Alvarado, Carmen Avendano, Jean Rodriguez and J. Carlos Menendez. Org. Lett. 2005, 7, 2197-2200

Lipases-Catalyzed Enantioselective Synthesis of Monocyclic Natural Products

H. Monti, G. Audran, Mini-Reviews in Organic Chemistry (MROC) 2005, 2, 265-281.

Straightforward Enantioselective Synthesis of (+)-ancistrofuran.

E. Palombo, G. Audran, H. Monti, Tetrahedron 2005, 61, 9545-9549.

Azaindoles as medicinally relevant scaffolds.

J. Rodriguez, M. Feraud Spec. Chem. Mag.2005, 12, 16.

Aliphatic and Alicyclic Ketones (except Cyclobutanones and Cyclopropanones): Synthesis by Fragmentation and Rearrangement

T. Constantieux, J. Rodriguez. Science of Synthesis, Volume 26, J. Cossy, Ed., Georg Thieme Verlag (Stuttgart), 2005, 413-462.

Mild oxidative one-carbon homologation of aldehyde to amide

D. Bonne,M. Dekhane, J. Zhu, J. Am. Chem. Soc. 2005, 127, 6926-6927.

The Formation of Silylated b-Lactams from Silylketenes through Lewis Acid Promoted [2+2] Cycloadditions : A Combined Theoretical and Experimental Study.

B. Pelotier, M. Rajzmann, J.-M. Pons, P. Campomanes, R. Lopez et T.L. Sordo Eur. J. Org. Chem. 2005, 2599-2606.

Chemoenzymatic Taxanes Approach Using Both Enantiomers of the Same Building Block. Part 2: Taxol® CD ring unit

J.-P. Uttaro, G. Audran, H. Monti, J. Org. Chem. 2005, 70, 3484-3489.

Multicomponent Domino Reaction from b-Ketoamides: Highly Efficient Access to Original Polyfunctionalized 2,6-Diazabicyclo[2.2.2]octane Cores.

Frédéric Liéby-Muller, Thierry Constantieux, and Jean Rodriguez J. Am. Chem. Soc. 2005, 127, 17176-17177.

Exploiting the dual reactivity of o-isocyanobenzamide : three component synthesis of 4-imino-4H-3,1-benzoxazines

D. Bonne, M. Dekhane, J. Zhu, J. Org. Lett. 2005, 7, 5285-5288

Azaindoles: Provence Technologies et PCAS s’allient.

Jean Rodriguez Industrie Pharma Magazine2005, 17, 10.

An Operationally Simple Base-Catalyzed Multi- component Domino Transfor-mation: Stereoselective Preparation of Trisubstituted Alkenes and 1,3-Dienes.

Hadjira Habib-Zahmani, Salih Hacini, Cédric Bories, Robert Faure, Jean Rodriguez Synthesis 2005, 2151-2156

Multicomponent Reactions with 1,3-Dicarbonyl Derivatives: Applications to the Synthesis of Polyfunctionalized Heterocycles.

T. Constantieux, J. Rodriguez dans : « Targets in Heterocyclic Systems » Vol 9, 2005.

Enantioselective Synthesis of (+)-Ricciocarpin A Using an Auxiliary Hydroxyl Group and a Diastereofacial Selectivity Based Methodology

E. Palombo, G. Audran, H. Monti, Synlett 2005, 2104-2106.

Azaindoles: Provence Technologies et PCAS mettent leurs forces en commun.

Jean Rodriguez Chimie Pharma Hebdo2005, 312, 4.

Enantioselective synthesis of natural (-)-tochuinyl acetate, (-)-dihydrotochuinyl acetate and (+)-b-cuparenone using both enantiomers of the same building block

S. Acherar, G. Audran, H. Monti, Tetrahedron 2004, 60, 5907-5912.

Utilization of Nonionic Bases in Water as a Highly Efficient Organocatalytic System for Michael Addition of b-Ketoesters.

D. Bensa, J. Rodriguez Synthetic Commnunications 2004, 34, 1515-1533, 2004

Stereoselective Synthesis of Bicyclo[4.2.1]nonane Skeletons by Ring-Closing Metathesis: A New Versatile Methodology for the Efficient Assembly of Functionalized Cyclooctanoids

Antoine Michaut, Sonia Miranda-Garcia, J. Carlos Menendez,Jean Rodriguez Org. Lett. 2004, 6, 3075-3078

The b-Lactone Route to a,b-Unsaturated d-Lactones. Total Syntheses of Goniothalamine and (-)-Massoialactone.

L. Fournier, P.J. Kocienski et J.-M. Pons Tetrahedron 2004, 60, 1659-1663.

P-BEMP: a New Efficient and Commercially Available User-friendly and Recyclable Heterogeneous Organocatalyst for the Michael Addition of 1,3-Dicarbonyl Compounds.

D. Bensa, T. Constantieux, J. Rodriguez. Synthesis, 2004, 923-027

A tehrmochromism study in th feerrocenyl-benzopyran series

S. Anguille, P. Brun, R. Guglielmetti Appl. Organomet. Chem., 2004, 18, 68-70.

Unprecedented in Situ Oxidative Ring Cleavage of Isoxazolidines: Diastereoselective Transformation of Nitronic Acids and Derivatives into 3-Hydroxymethyl 4-Nitro Tetrahydrofurans and Pyrrolidines.

Pierre-Yves Roger, Anne-Catherine Durand, Jean Rodriguez, Jean-Pierre Dulcère Org. Lett. 2004, 6, 2027-2029

Facile, Efficient and Chemoselective Palladium(0)-Catalyzed Isomerization of 2-Vinylidenehydrofurans into Valuable Functionalized 1,3-Dienes

Laurence Wavrin, Cyril Nicolas, Jacques Viala, Jean Rodriguez Synlett 2004, 1820-1822

Ammonium chloride promoted Ugi four-component, five-centre reaction of ?-substituted ?-isocyanoacetic acid : a strong solvent effect

D. Bonne,M. Dekhane, J. Zhu, J. Org. Lett. 2004, 6, 4771-4774.

Utilisation of 1,3-Dicarbonyl Derivatives in Multicomponent Reactions

Celine Simon, Thierry Constantieux, and Jean Rodriguez Eur. J. Org. Chem. 2004, 4957-4980.

From the MARDi Cascade to the Stereoselective Construction of Functionalized Bicyclo[5.4.0]undecene Skeletons Occurring in Natural Compounds

Marie-Hélène Filippini, jean Rodriguez Letters in Organic Chemistry 2004, 1, 53-54.

Silylketenes under Kulinkovich Conditions : alkene / ketene exchange vs nucleophilic addition. Application to the stereoselective preparation of vinylcyclopropanols.

E. Raponi et J.-M. Pons Tetrahedron Lett. 2003, 44, 9193-9196.

Efficient synthesis of spirolactones from cyclic anhydrides via an allylation-cycloisomerisation Sequence

M. Michaut, M. Santelli, J.-L. Parrain, Tetrahedron Lett. 2003, 44, 2157-2159

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