Jérôme Yves Cassayre
Syngenta
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Publication
Featured researches published by Jérôme Yves Cassayre.
Angewandte Chemie | 2002
Jérôme Yves Cassayre; Fabien Gagosz; Samir Z. Zard
A short and efficient total synthesis of (±)-13-deoxyserratine (3) features a highly stereoselective intramolecular Pauson-Khand reaction of 1 and a cascade of radical cyclizations starting with the amidyl radical 2. The desired alkaloid 3 was thus obtained in ten steps in an overall yield of 12 %. THP = tetrahydropyranyl, TBS = tert-butyldimethylsilyl.
PLOS ONE | 2012
Ann E. Sluder; Sheetal Shah; Jérôme Yves Cassayre; Ralph Clover; Peter Maienfisch; Louis-Pierre Molleyres; Elizabeth A. Hirst; Anthony J. Flemming; Min Shi; Penny Cutler; Carole Stanger; Richard Spurring Roberts; David Hughes; Thomas Flury; Mike Robinson; Elke Maria Hillesheim; Thomas Pitterna; Fredrik Cederbaum; Paul Anthony Worthington; Andrew J. Crossthwaite; John Windass; Richard A. Currie; Fergus Gerard Paul Earley
The efficacy of all major insecticide classes continues to be eroded by the development of resistance mediated, in part, by selection of alleles encoding insecticide insensitive target proteins. The discovery of new insecticide classes acting at novel protein binding sites is therefore important for the continued protection of the food supply from insect predators, and of human and animal health from insect borne disease. Here we describe a novel class of insecticides (Spiroindolines) encompassing molecules that combine excellent activity against major agricultural pest species with low mammalian toxicity. We confidently assign the vesicular acetylcholine transporter as the molecular target of Spiroindolines through the combination of molecular genetics in model organisms with a pharmacological approach in insect tissues. The vesicular acetylcholine transporter can now be added to the list of validated insecticide targets in the acetylcholine signalling pathway and we anticipate that this will lead to the discovery of novel molecules useful in sustaining agriculture. In addition to their potential as insecticides and nematocides, Spiroindolines represent the only other class of chemical ligands for the vesicular acetylcholine transporter since those based on the discovery of vesamicol over 40 years ago, and as such, have potential to provide more selective tools for PET imaging in the diagnosis of neurodegenerative disease. They also provide novel biochemical tools for studies of the function of this protein family.
Bioorganic & Medicinal Chemistry | 2009
Thomas Pitterna; Jérôme Yves Cassayre; Ottmar Franz Hüter; Pierre M. J. Jung; Peter Maienfisch; Fiona Murphy Kessabi; Laura Quaranta; Hans Tobler
Archive | 2005
Peter Maienfisch; Louis-Pierre Molleyres; Jérôme Yves Cassayre; Fredrik Cederbaum; Camilla Corsi; Thomas Pitterna
Archive | 2011
Nicholas Phillip Mulholland; Edouard Godineau; Jérôme Yves Cassayre; Peter Renold; Qacemi Myriem El; Guillaume Revol
Archive | 2010
Jérôme Yves Cassayre; Peter Renold; Myriem El Qacemi; Thomas Pitterna; Julie Clementine Toueg
Archive | 2009
Michel Muehlebach; Thomas Pitterna; Jérôme Yves Cassayre; Andrew Edmunds; Camilla Corsi; Qacemi Myriem El; Roger Graham Hall; André Jeanguenat; André Stoller; Christopher Richard Ayles Godfrey; Juergen Schaetzer; Olivier Loiseleur; Peter Maienfisch; Neil Brian Carter
Archive | 2009
Michel Muehlebach; Thomas Pitterna; André Jeanguenat; Qacemi Myriem El; Roger Graham Hall; Andrew Edmunds; Camilla Corsi; André Stoller; Christopher Richard Ayles Godfrey; Juergen Schaetzer; Olivier Loiseleur; Peter Maienfisch; Jérôme Yves Cassayre
Archive | 2012
Jérôme Yves Cassayre; Elvira Molitor
Archive | 2012
Qacemi Myriem El; Jérôme Yves Cassayre; Julie Clementine Toueg; Peter Renold; Thomas Pitterna