Honoré Monti

Centre National de la Recherche Scientifique — France

Chemistry · Physical Sciences

14h-index482citations59works0.02yr avg
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Research Topics

Synthetic Organic Chemistry Methods(19), Asymmetric Synthesis and Catalysis(17), Chemical synthesis and alkaloids(12), Carbohydrate Chemistry and Synthesis(10), Asymmetric Hydrogenation and Catalysis(9)

Publications59 total

Synthesis and Antiviral Evaluation of (-)-3′-Methylcarbovir, (-)-3′-Methylabacavir, and Modified Purine Analogues
Synthesis·2008
Stereoselective Synthesis ofNovel Aristeromycin Analogues as Potential Antiviral Agents
Synthesis·2008· 2 cited
Highly Efficient Stereocontrolled Synthesis of Danishefsky’s Taxol CD Ring Key Intermediate
The Journal of Organic Chemistry·2008· 5 cited
Chemoenzymatic synthesis and antiviral evaluation of conformationally constrained and 3′-methyl-branched carbanucleosides using both enantiomers of the same building block
Bioorganic & Medicinal Chemistry·2007· 5 cited
First Enantioselective Synthesis and Absolute Stereochemistry Assignment of New Monoterpene Aldehyde‐Esters from <i>Bupleurum gibraltaricum</i>
European Journal of Organic Chemistry·2007· 5 cited
Total Chemoenzymatic Synthesis of (-)-3′-Methylaristeromycin
Synlett·2007· 1 cited
Chemoenzymatic synthesis of novel adenosine carbanucleoside analogues containing a locked 3′-methyl-2′,3′-β-oxirane-fused system
Tetrahedron·2007· 5 cited
Conformationally Locked Carbocyclic Nucleosides: Synthesis of the 1-Methyl-6-oxabicyclo[3.1.0]hexane Scaffold
Synlett·2006
Improved Enantioselective Synthesis of Natural Striatenic Acid and Its Methyl Ester.
ChemInform·2006
Improved enantioselective synthesis of natural striatenic acid and its methyl ester
Tetrahedron Letters·2006· 16 cited
Enantioconvergent Access to the Enantiomerically Pure Building Blocks (+)- or (-)-4-Hydroxy-3-methyl-2-cyclohexenone Using a Chemoenzymatic Process
Synlett·2006· 2 cited
Lipase‐Promoted Enantioselective Syntheses of Monocyclic Natural Products
ChemInform·2006
Straightforward Enantioselective Synthesis of (+)‐Ancistrofuran.
ChemInform·2005
Enantioselective Synthesis of (+)‐Ricciocarpin A Using an Auxiliary Hydroxyl Group and a Diastereofacial Selectivity Based Methodology.
ChemInform·2005· 3 cited
Straightforward enantioselective synthesis of (+)-ancistrofuran
Tetrahedron·2005· 14 cited
Lipases-Promoted Enantioselective Syntheses of Monocyclic Natural Products
Mini-Reviews in Organic Chemistry·2005· 7 cited
Chemoenzymatic Taxanes Approach Using Both Enantiomers of the Same Building Block. 2. Taxol CD Ring Unit
The Journal of Organic Chemistry·2005· 14 cited
Enantioselective Synthesis of (+)-Ricciocarpin A Using an Auxiliary Hydroxyl Group and a Diastereofacial Selectivity Based Methodology
Synlett·2005· 1 cited
Lipase‐Promoted Access to Phenolic Herbertane‐Type Sesquiterpenes: (+)‐1,14‐Herbertenediol, (−)‐α‐Herbertenol, (−)‐Herbertenediol and Their Enantiomers
European Journal of Organic Chemistry·2004· 12 cited
Enantioselective synthesis of natural (−)-tochuinyl acetate, (−)-dihydrotochuinyl acetate and (+)-β-cuparenone using both enantiomers of the same building block
Tetrahedron·2004· 18 cited
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Frequent Co-authors

Gérard Audran(38), G. LEANDRI(12), Jean‐Marie Galano(8), Jean‐Pierre Monti(6), Elie Palombo(6), Yoann Aubin(5), Jean‐Pierre Uttaro(5), Gilles Laval(4), Samir Acherar(4), Paul Brémond(4), Michel Féraud(3), Denis Rizzotto(2), Nicolas Vanthuyne(2), Patrick Charles(2), Erik De Clercq(2), MARCEL BERTRAND(2), Kenji Mori(1), Nicolas Tiliacos(1), Robert Faure(1), Fabrice Cecchin(1)