Leon Ghosez, Ph.D.

Affiliations: 
Organic & Medicinal Chemistry Institut Européen de Chimie et Biologie 
Area:
total synthesis, synthetic methods, electrophilic catalysis, serine proteases, medicinal chemistry
Website:
http://www.iecb.u-bordeaux.fr/index.php/en/equipes/70-organic-a-medicinal-chemistry
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"Leon Ghosez"
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Publications

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Badarau E, Reddy HV, Loudet A, et al. (2020) Productive Syntheses of Privileged Scaffolds Inspired by the Recognition of a Diels-Alder Pattern Common to three Classes of Natural Products. Chemistry (Weinheim An Der Bergstrasse, Germany)
Gati W, Munyemana F, Colens A, et al. (2020) A mild method for the replacement of a hydroxyl group by halogen: 2. unified procedure and stereochemical studies Tetrahedron. 76: 131441
Munyemana F, George I, Devos A, et al. (2016) A mild method for the replacement of a hydroxyl group by halogen. 1. Scope and chemoselectivity Tetrahedron. 72: 420-430
Ghosez L, Marko I. (2011) Heinz Günther Viehe (1929-2010) Angewandte Chemie. 123: 3413-3414
Ghosez L, Sainte F, Rivera M, et al. (2010) Synthesis and reactions of 3-alkoxy-2H-azirines Recueil Des Travaux Chimiques Des Pays-Bas. 105: 456-461
DE TOLLENAERE C, GHOSEZ L. (2010) ChemInform Abstract: Synthesis and Cycloadditions of 1-[(tert-Butyldimethylsilyl)oxy]alkenyl Isocyanates. Cheminform. 29: no-no
Marchand-Brynaert J, Ferroud D, Serckx-Poncin B, et al. (2010) Synthesis and Stability of Functionalized Epoxides Topologically Related To Beta-lactam Antibiotics Bulletin Des SociéTéS Chimiques Belges. 99: 1075-1084
Marchand-Brynaert J, Vanlierde H, Ghosez L. (2010) Bicyclic imidazolidinones as potential antibiotics Bulletin Des SociéTéS Chimiques Belges. 97: 1081-1094
Srinivas K, Kauffmann B, Dolain C, et al. (2008) Remote substituent effects and regioselective enhancement of electrophilic substitutions in helical aromatic oligoamides. Journal of the American Chemical Society. 130: 13210-1
Ghosez L, Yang G, Cagnon JR, et al. (2004) Synthesis of enantiomerically pure α-amino-β-hydroxy- cyclobutanone derivatives and their transformations into polyfunctional three- and five-membered ring compounds Tetrahedron. 60: 7591-7606
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