Contact details

Professor at the University of Reims Champagne-Ardenne

Faculty of Exact and Natural Sciences

Institute of Molecular Chemistry - ICMR UMR CNRS 7312
Campus du Moulin de La Housse BP 1039 51687 REIMS Cedex 2
Phone : 00 33 3.26.91.32.36
E-Mail : arnaud.haudrechy@univ-reims.fr

Website: ICMR

Key words

Sugars; natural substances synthesis

International programmes

Creation of the Glycolipid European Network (GLEN)

International conferences

- Synthèse Totale de l’Huperzine A, SECO, le 25/5/00 à Houffalize
- Sur la Route de la Fumagilline, le 22/4/03 à Montréal (UQAM)
- On the Road to Fumagillin, le 23/4/03 à Montréal (Concordia University)
- Two stimulating concepts in natural substances synthesis: the NEO cascade and the CIM strategy, 30 juin au 2 juillet 2010, International Conference on Medicinal Chemistry, Reims.

- A stimulating concept in natural substances synthesis: the CIM strategy, 23 novembre 2011, Queen’s University, Belfast.

Main publications

- Cyclization of Hydroxy Enol Ethers : A Stereocontrolled Approach To 3-deoxy-D-Manno-2-octulosonic Acid containing Disaccharides, A. Haudrechy and P. Sinaÿ*, J. Org. Chem., 1992, 57, 4142

- Preferred Conformations of C-Glycosides, 14. Synthesis and Conformational Analysis of Carbon Analogs of the Blood Group Determinant H-Type II, A. Wei, A. Haudrechy, C. Audin, H.-S. Jun, N. Haudrechy-Bretel and Y. Kishi*, J. Org. Chem., 1995, 60, 2160

- Analysis of the Diastereoselectivity of a Diels-Alder Cycloaddition through 2H NMR in chiral liquid crystals, A. Meddour, A. Haudrechy, P. Berdagué, W. Picoul, Y. Langlois and J. Courtieu, Tetrahedron: Asymmetry, 1996, 7, 2489

- A Simple Method of Drawing Stereoisomers From Complicated Symmetrical Structures, A. Haudrechy, J. Chem. Ed., 2000, 864

- A Formal Synthesis of (+)-Huperzin A, C. Chassaing, A. Haudrechy, C. Riche and Y. Langlois*, Tetrahedron, 2000, 56, 3181

- A Stereoselective Formal Synthesis of Fumagillin, O. Bedel, A. Haudrechy*, Y. Langlois*, Eur. J. Org. Chem., 2004, 3813

- Highly Enantioselective Sequential Claisen-Ireland / Metathesis: Synthesis of Cycloalkenes Bearing two Contiguous Highly Functionalized Asymmetric Centers, A. Français, O. Bedel,
W. Picoul, A. Meddour, J. Courtieu and A. Haudrechy*, Tetrahedron Asymmetry, 2005, 16, 1141

- Diastereoselective Access to the Spirotetronate Subunit of the Quartromicins, O. Bedel*, A. Français and A. Haudrechy*, Synlett, 2005, 15, 2313

- Selective Synthesis of a-C-(alkynyl)-Galactosides by an Efficient Tandem Reaction, S. Guillarme, K. Plé and A. Haudrechy*, J. Org. Chem., 2006, 71, 3, 1015

- Alkynylation of Chiral Aldehydes: Alkoxy-, Amino- and Thioaldehydes, S. Guillarme, K. Plé*, A. Banchet, A. Liard and A. Haudrechy*, Chem. Reviews, 2006, 106(6); 2355

- Quiral: a Computer Program for the Synthesis of Chiral Molecules from Sugars, J.-M. Nuzillard and A. Haudrechy, Tetrahedron Letters, 2007, 48, 13, 2311-2313

- Is Osmylation Always Preferring the Richest Double Bond?, A. Français, O. Bedel, A. Haudrechy*, Tetrahedron, 2008, 2495

- Molecular Dynamics Simulation Study on the Interaction of KRN 7000 and three analogues with Human CD1d, E. Hénon*, M. Dauchez, A. Haudrechy, A. Banchet, Tetrahedron, 2008, 9480

- D-C-Mannopyranosides, M. Choumane, A. Banchet, N. Probst, S. Gérard, K. Plé*, A. Haudrechy*, Comptes Rendus de Chimie, 2011, 14, 2-3, 235

- The stimulating adventure of KRN 7000, A. Banchet-Cadeddu, E. Hénon, M. Dauchez,J.-H. Renault, F. Monneaux,A. Haudrechy, Org. Biomol. Chem., 2011, 9, 3080

- The Chemistry of L-Sorbose, I. Zebiri, S. Balieu, A. Guilleret, R. Reynaud, A. Haudrechy, Eur. J. Org. Chem., 2011, 16, 2905

- A further contribution to the study of Sagittamide A: Synthesis of a pivotal intermediate belonging to a rare L-series, A. Humbert, K. Plé, D. Harakat, A. Martinez, A. Haudrechy, Molecules, 2012, 17, 7, 7709-7721

- Stereoselective synthesis of (2S,3S,4R,5S)-2,5-dihydroxymethyl-3,4-dihydroxypyrrolidine derivatives from L-Sorbose, S. Balieu, A. Guilleret, R. Reynaud, A. Haudrechy, Carb. Res., 2013, 374, 14-22

- Are the furanosides that flexible? A Ring Dihedral Principal Component Analysis of furanose conformation, C. Coiffier, C. Barberot, J.-M. Nuzillard, P. Goekjian, E. Hénon, A.Haudrechy, Carbohydrate Chem., 2014, 40, 378-400.

- From D-Xylose to a D-Glycero-L-altrose derivative, A. Banchet-Cadeddu, A. Haudrechy, Tetrahedron Lett. 2014, 55, 4605-4607.