CV F.-D. Boyer

• Organic Chemistry
• Biochemistry
• Chemical Biology
• Plant sciences
• Strigolactone

82 publications – 3 book chapters

23 oral communications and conferences,

3 patents

1. Xolin, A. et al. Stereocontrolled glycoside synthesis by activation of glycosyl sulfone donors with scandium(iii) triflate. Org. Biomol. Chem. 16, 325-335, doi:10.1039/C7OB02792C (2018).
2. Boutet-Mercey, S. et al. Validated Method for Strigolactone Quantification by Ultra High-Performance Liquid Chromatography – Electrospray Ionisation Tandem Mass Spectrometry Using Novel Deuterium Labelled Standards. Phytochem. Anal. 29, 59-68, doi:10.1002/pca.2714 (2018).
3. Beau, J.-M. et al. Glycosylation: The Direct Synthesis of 2-Acetamido-2-Deoxy-Sugar Glycosides. Eur. J. Org. Chem. 2018, 5795-5814, doi:10.1002/ejoc.201800735 (2018).
4. Berthelot, N. et al. Synthesis of lipo-chitooligosaccharide analogues and their interaction with LYR3, a high affinity binding protein for Nod factors and Myc-LCOs. Org. Biomol. Chem. 15, 7802-7812, doi:10.1039/C7OB01201B (2017).
5. Xolin, A. et al. Iron(III)-Triflate-Catalyzed Multiple Glycosylations with Peracetylated β-d-Glucosamine. Eur. J. Org. Chem., 3408-3418, doi:10.1002/ejoc.201600457 (2016).
6. Gillard, L. et al. Chitooligosaccharide Synthesis Using an Ionic Tag. Eur. J. Org. Chem., 1103-1109, doi:10.1002/ejoc.201501476 (2016).
7. de Saint Germain, A. et al. An histidine covalent receptor and butenolide complex mediates strigolactone perception. Nat. Chem. Biol. 12, 787-794, doi:10.1038/nchembio.2147 (2016).
8. Lopez-Obando, M. et al. Strigolactone biosynthesis and signaling in plant development. Development 142, 3615-3619, doi:10.1242/dev.120006 (2015).
9. Xolin, A. et al. Glycosylation with N-acetyl glycosamine donors using catalytic iron(iii) triflate: from microwave batch chemistry to a scalable continuous-flow process. Org. Chem. Front. 1, 992-1000, doi:10.1039/c4qo00183d (2014).
10. Boyer, F.-D. et al. New Strigolactone Analogs as Plant Hormones with Low Activities in the Rhizosphere. Molecular Plant 7, 675-690 (2014).
11. Gillard, L. et al. Synthesis of the Fungal Lipo-Chitooligosaccharide Myc-IV (C16:0, S), Symbiotic Signal of Arbuscular Mycorrhiza. Eur. J. Org. Chem., 7382-7390, doi:10.1002/ejoc.201301015 (2013).
12. de Saint Germain, A. et al. Novel insights into strigolactone distribution and signalling. Curr. Opin. Plant Biol. 16, 583-589, doi:http://dx.doi.org/10.1016/j.pbi.2013.06.007 (2013).
13. Chen, V. X. et al. New Synthesis of A-Ring Aromatic Strigolactone Analogues and Their Evaluation as Plant Hormones in Pea (Pisum sativum). Chem. – Eur. J. 19, 4849-4857, doi:10.1002/chem.201203585 (2013).
14. Boyer, F.-D. et al. Structure-activity relationship studies of strigolactone-related molecules for branching inhibition in garden pea: molecule design for shoot branching. Plant Physiol. 159, 1524-1544, doi:10.1104/pp.112.195826 (2012).
15. Stévenin, A. et al. Regioselective Control in the Oxidative Cleavage of 4,6-O-Benzylidene Acetals of Glycopyranosides by Dimethyldioxirane. J. Org. Chem. 75, 1783-1786, doi:10.1021/jo9026098 (2010).
16. Chen, V. X. et al. Stereochemistry, Total Synthesis, and Biological Evaluation of the New Plant Hormone Solanacol. Chem. – Eur. J. 16, 13941-13945, doi:10.1002/chem.201002817 (2010).

Catherine Rameau and Sandrine Bonhomme (IJPB, UMR 1318 INRA/AgroParisTech)

Jean-Bernard Pouvreau/Philippe Delavault (Université de Nantes, Laboratoire de Biologie et Pathologies végétales EA1157)

Soizic Rochange/Guillaume Bécard (UMR 5546 Université de Toulouse/CNRS),

Sofie Goormachtig (VIB, Belgium)

Jean-Jacques Bono (LIPM, INRA Toulouse)

Doctor Henri Labbé and Mrs Henri Labbé Prize (2023)

Annual prize for biological chemistry and nutrition from the French Académie des Sciences

Coordinator of Scientific Platforms and Services at ICSN.

About 80 hours per year of organic chemistry at the IUT of Paris-Saclay University.

2018-present: Teaching at Agroparistech 3rd year, « From plant to drug ».