Publications avant 2011

2010

  •  C. Hulot, J. Peluso, G. Blond, C. Muller, J. Suffert
    Biorg. Med. Chem. Letters 2010, 20, 6836-6839
    Synthesis and biological activity of exotic polycycles such as cyclooctatrienes and fenestranes

2009

  • C. Hulot, S. Amiri, G. Blond, P. Schreiner, J. Suffert
    J. Am. Chem. Soc.
    2009, 131, 13387

    Understanding the Torquoselectivity in 8p-Electrocyclic Cascade Reactions: Synthesis of Fenestrenes versus Cyclooctatrienes

2008

  • C. Hulot, G. Blond, J. Suffert
    J. Am. Chem. Soc.
     2008, 130, 6046
    8
    p-6p-[O2-oxi]-Cyclization Cascade: a Unique Synthesis of New [4.6.4.6] Fenestradienes and [4.6.4.6] Fenestrenes
    Article Highlighté in C&EN
    2008, 86, 26. Science and Technology concentrates "Fenestrane in a Snap"

  • G. Blond, C. Bour, B. Salem, J. Suffert
    Org. Letters. 2008
    , 10, 1075-1078
    A New Pd-catalyzed Cascade Reaction to the Synthesis of Exotic and Aromatic Polycycles

2006

  • C. Bour, J. Suffert
    Eur. J. Org. Chem. 2006, 1391
    4-Exo-dig Cyclocarbopalladation: A Straightforward Synthesis of Cyclobutane diols from Acyclic g-Bromopropargylicdiols under Microwaves Irradiation

  • C. Bour, G. Blond, B. Salem, J. Suffert
    Tetrahedron 2006, 62, 10567-10581
    4-exo-dig and 5-exo-dig Cyclocarbopalladation: an E
    xpeditious Solution toward Molecular Complexity?

2005

  • C. Bour , J. Suffert
    Org. Lett. 2005, 7, 653
    Cyclocarbopalladation: Sequential Cyclization and CH Activation/Stille Cross-Coupling in the Pd-5-Exo-Dig Reaction                       

  • A. Mota, A. Dedieu, C. Bour , J. Suffert
    J. Am. Chem. Soc. 2005, 127, 7171
    Cyclocarbopalladation Reactions Involving an Unusual 1,5-Palladium Vinyl to Aryl Shift as Termination Step: Theoretical Study of the Mechanism

2004

  • B. Salem, P. Klotz, J. Suffert
    Synthesis
    (Feature Article, sur invitation), 2004, 2, 298
    Cascade Cyclization via a 4-exo-dig Cyclocarbopalladation for an Easy Access to New Polycyclic Structures

  • B. Salem, J. Suffert
    Angew. Chem. Int. Ed. 2004, 43, 2826
    4-Exo-dig Cyclocarbopalladation/8
    p-Electrocyclization Cascade: an Expeditious Access to the Tricyclic Core Strutures of Ophiobolins and Aleurodiscal

2003

  • B. Salem, P. Klotz, J. Suffert
    Org. Lett.
    , 2003, 5, 845-848
    Cyclocarbopalladation: Formation of Bicyclic1,2
    Cyclobutanediols through a Rare 4-exo-dig Cyclization

  • B. Salem, E. Delort,  P. Klotz, J. Suffert
    Org. Lett., 2003, 5, 2307-2310
    Cyclocarbopalladation: 5-exo-dig Cyclization Versus Direct Stille Cross Coupling Reaction. The Influence of the a,b-Propargylic Substitution

  • C. Goze,D. V. Kozlov,F. N. Castellano, J. Suffert and R. Ziessel
    Tetrahedron Lett.
    , 2003, 44, 8713
    Bipyridine and Terpyridine Based Ruthenium Metallosynthons for Grafting of Multiple Pyrene Auxiliaries

2002

  • E. Abraham, J. Suffert
    Synlett
    , 2002, 328-330
    In Situ Generation of 1-Propyne: a Useful Introduction of 1-Propyne on Unsaturated Halogenated Compounds through the Sonogashira Reaction

  • C. Morice, F. Garrido, A. Mann, J. Suffert
    Synlett
    , 2002, 501-503
    Palladium Assisted Substitution of 3-Benzo[b]furan Triflates

  • S. Brückner, E. Abraham, P. Klotz, J. Suffert
    Org. Letters
    , 2002, 4, 3391-3393
    Cascade Cyclization : an Easy Access to Highly Unsaturated Polycyclic Ring System trrough a New Tandem Stille/[4+2] Reaction under Mild Conditions

2001

  • C. Morice, M. Domostoj, K. Brinner, A. Mann, J. Suffert, C.-G. Wermuth
    Tetrahedron Lett.
    , 2001, 42, 6499-6502
    Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions

  • J. Suffert, B. Salem, P. Klotz
    J. Am. Chem. Soc.,
    2001, 123, 12107-12108
    Cascade Cyclization: Carbopalladative Cyclization Followed by Electrocyclic Closure as a Route to Complex Polycycles     

2000

  • J. Suffert, S. Raeppel, F. Raeppel, B. Didier
    Synlett
    , 2000, 874-876
    Straightforward Acces to [6]Metacyclophene-based Enynes by an Inter-intramolecular Tandem Etherification through a One-Pot Double SNAr Reaction