Riccardo PICCARDI

Research Scientist, CNRS

Laboratoire de Chimie et Biochimie pharmacologiques et toxicologiques (LCBPT) – CNRS UMR 8601
Université Paris Descartes
45 Rue des Saints Pères
75270 Paris Cedex 06
France

Laboratoire de Chimie et Biochimie
Pharmacologiques et Toxicologiques (LCBPT)
CNRS UMR 8601
Université Paris Descartes
45 Rue des Saints Pères
75270 Paris Cedex 06
France

Curriculum Vitae

Academic and Professional Background 

2014-  CNRS Researcher. UMR 8601, University of Paris Descartes.
2009- 2014  CNRS Researcher. UMR 8182, University of Paris Sud.
2008-2009 Temporary Associate Professor (ATER). UMR 8182, University of Paris Sud.
2006-2008 Post-Doctoral Fellow University of Claude Bernard Lyon I (with Prof. O. Baudoin)
2005-2006 Post-Doctoral Fellow Technical University of Munich (TUM)-Germany (with Prof. T. Bach)
2001-2005 Ph.D. in chemistry. University of Bern-Switzerland (with Prof. P. Renaud)
2000-2001 Master in Chemistry (Laurea). University of Florence -Italy (with Dr. G. Reginato)

Fundings:

2024 IdEX “Emergence” Université paris Cité (projet Light Carbenes)
2010  “Atractivité ” Université Paris Sud-11

Réseaux

GdR Synthflux

 

Collaborations:

Pr. Emmanuelle SACHON (Laboratoire de Biomolécules -Sorbonne Université -ENS)

Teaching

– Introduction to flow chemistry (2h intervention during Green Chemistry teaching unit)

– “Travaux Dirigés” LASS (minor chemistry)

 

Administratives tasks

Health and safety assistant

– Webmaster

 

Languages

French

ENglish

Italian

Research

The reserch I am developing is focused on two main subjects:

– the reactivity of α-alkynyl-diazosilanes: a very interesting new class of compounds that can react easily with carboxylic acids and can be also used in the functionalisation of proteins in biological media.

 

 

– the reactivity of dimethylalkynylaluminum reagents and continuous flow reactions

 

Publications

2024
  1. T. Zhao, E. Sachon, L. Micouin, R. Piccardi α-Silylated Diazoalkynes: New Tools for Bioconjugation of Proteins” 2024, 30, e202302807.
    DOI: 10.1002/chem.202302807
  2. L. Micouin, R. Piccardi, Organoaluminum Reagents, in Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, Elsevier, 2024, ISBN 9780124095472, DOI: 10.1016/B978-0-323-96025-0.00041-7.
2019
  1. Zhao, L. Micouin, R. Piccardi. “Synthesis of Organometallic Compounds in Flow”. Helv. Chim. Acta, 2019⟨10.1002/hlca.201900172⟩.
2018
  1. Piccardi, S. Turcaud, E. Benedetti, L. Micouin. “Synthesis and Reactivity of Mixed Dimethylalkynylaluminum Reagents”. Synthesis, 2018, 51, 97-106. ⟨10.1055/s-0037-1610392⟩.
  2. Zhao, R. Piccardi, L. Micouin. “Rapid and Effective Synthesis of α-Acyloxy-α-alkynyltrimethylsilanes”. Org. Lett. 2018, 20, 5015-5018. ⟨10.1021/acs.orglett.8b02165⟩.
2016
  1. R. Piccardi, A. Coffinet, E. Benedetti, S. Turcaud, L. Micouin, “Continuous flow synthesis of dimethylalkynylaluminum reagents” Synthesis 2016, 48, 3272-3278
  2. R. Piccardi, L. Micouin, O. Jackowski “The Chemistry of Alkynylaluminum Species”. I. Marek Ed. PATAI’S Chemistry of Functional Groups, John Wiley & Sons, Ltd, 1-47, 2016, DOI: https://doi.org/10.1002/9780470682531.pat0832
Older publications
  1. Prosa, R. Turgis, R. Piccardi, M.-C. Scherrmann, “Soluble Polymer-Supported Flow Synthesis: A Green Process for the Preparation of Heterocycles” Eur. J. Org. Chem. 2012, 2188-2200
  2. Chaumontet, R. Piccardi, O. BaudoinSynthesis of 3,4-Dihydroisoquinolines by a C(sp3)–H Activation-Electrocyclization Strategy: Total Synthesis of Coralydine” Angew. Chem. Int. Ed. 2009, 48, 179-182
  3. Chaumontet, R. Piccardi, N. Audic, J. Hitce, J.-L. Peglion, E. Clot, O. Baudoin, “Synthesis of Benzocyclobutenes by Palladium-Catalyzed C−H Activation of Methyl Groups: Method and Mechanistic Study” J. Am. Chem. Soc. 2008, 130, 15157 – 15166 
  4. Piccardi, P. Renaud, “Formal Synthesis of (+) and (-)-Ferruginine” Eur. J. Org. Chem. 2007, 10, 4752-4757.
  5. Reginato, A. Mordini, M. Valacchi, R. PiccardiSynthesis of non-racemic b-branched a-(aminoalkyl)-acrylates from naturally occurring amino acids” Tetrahedron: Asymmetry 2002, 13, 595-600