← Back to directory

Giovanni Poli

Researcher Next ID · RN-041109

Researcher · Chemistry

Centre National de la Recherche Scientifique

Paris, Portugal

Accepting doctoral researchersFunding unknown
Works count
394
Citation count
6,515
H-index
40
i10-index
155

Research interests

Chemistry
Asymmetric Synthesis and Catalysis
Catalytic C–H Functionalization Methods
Synthetic Organic Chemistry Methods
Catalytic Cross-Coupling Reactions
Asymmetric Hydrogenation and Catalysis

Publications

  • Free Fatty Acids Signature in Human Intestinal Disorders: Significant Association between Butyric Acid and Celiac Disease

    Nutrients · 2021 · 10.3390/nu13030742

  • Free Fatty Acids Signature in Human Intestinal Disorders: Significant Association between Butyric Acid and Celiac Disease

    Nutrients · 2021 · 10.3390/nu13030742

  • Platelets Promote Thromboinflammation in SARS-CoV-2 Pneumonia

    Arteriosclerosis Thrombosis and Vascular Biology · 2020 · https://doi.org/10.1161/atvbaha.120.315175

  • Evaluation and comparison of short chain fatty acids composition in gut diseases

    World Journal of Gastroenterology · 2019 · https://doi.org/10.3748/wjg.v25.i36.5543

  • Phenolic Profile and Susceptibility to Fusarium Infection of Pigmented Maize Cultivars

    Frontiers in Plant Science · 2018 · https://doi.org/10.3389/fpls.2018.01189

  • Metal-catalyzed C H activation/functionalization: The fundamentals

    Journal of Molecular Catalysis A Chemical · 2016 · https://doi.org/10.1016/j.molcata.2016.06.020

  • Synthesis of γ-Lactams and γ-Lactones via Intramolecular Pd-Catalyzed Allylic Alkylations

    Accounts of Chemical Research · 2014 · 10.1021/ar500178n

  • Direct Allylic Functionalization Through Pd‐Catalyzed C–H Activation

    European Journal of Organic Chemistry · 2014 · https://doi.org/10.1002/ejoc.201402049

  • Synthesis of γ-Lactams and γ-Lactones via Intramolecular Pd-Catalyzed Allylic Alkylations

    Accounts of Chemical Research · 2014 · 10.1021/ar500178n

  • Cavitand supported tetraphosphine: cyclodextrin offers a useful platform for Suzuki-Miyaura cross-coupling

    Chemical Communications · 2011 · 10.1039/c1cc12241j

  • Cavitand supported tetraphosphine: cyclodextrin offers a useful platform for Suzuki-Miyaura cross-coupling

    Chemical Communications · 2011 · 10.1039/c1cc12241j

  • Aryl Sulfoxides from Allyl Sulfoxides via [2,3]-Sigmatropic Rearrangement and Domino Pd-Catalyzed Generation/Arylation of Sulfenate Anions

    Organic Letters · 2009 · 10.1021/ol902620t

  • Aryl Sulfoxides from Allyl Sulfoxides via [2,3]-Sigmatropic Rearrangement and Domino Pd-Catalyzed Generation/Arylation of Sulfenate Anions

    Organic Letters · 2009 · 10.1021/ol902620t

  • Striking AcOH Acceleration in Direct Intramolecular Allylic Amination Reactions

    Chemistry - A European Journal · 2009 · 10.1002/chem.200901946

  • Striking AcOH Acceleration in Direct Intramolecular Allylic Amination Reactions

    Chemistry - A European Journal · 2009 · 10.1002/chem.200901946

  • Prevalence and type of pre‐analytical problems for inpatients samples in coagulation laboratory

    Journal of Evaluation in Clinical Practice · 2008 · 10.1111/j.1365-2753.2007.00875.x

  • Prevalence and type of pre‐analytical problems for inpatients samples in coagulation laboratory

    Journal of Evaluation in Clinical Practice · 2008 · 10.1111/j.1365-2753.2007.00875.x

  • Influence of temperature and time before centrifugation of specimens for routine coagulation testing

    International Journal of Laboratory Hematology · 2008 · 10.1111/j.1751-553x.2008.01058.x

  • Influence of temperature and time before centrifugation of specimens for routine coagulation testing

    International Journal of Laboratory Hematology · 2008 · 10.1111/j.1751-553x.2008.01058.x

  • Enantioselective Synthesis of Aryl Sulfoxides via Palladium-Catalyzed Arylation of Sulfenate Anions

    Organic Letters · 2007 · https://doi.org/10.1021/ol702343g

  • Quality and reliability of routine coagulation testing: can we trust that sample?

    Blood Coagulation & Fibrinolysis · 2006 · 10.1097/01.mbc.0000245290.57021.46

  • Aryl Sulfoxides via Palladium-Catalyzed Arylation of Sulfenate Anions

    Organic Letters · 2006 · https://doi.org/10.1021/ol062315a

  • Influence of the needle bore size on platelet count and routine coagulation testing

    Blood Coagulation & Fibrinolysis · 2006 · 10.1097/01.mbc.0000245300.10387.ca

  • Quality and reliability of routine coagulation testing: can we trust that sample?

    Blood Coagulation & Fibrinolysis · 2006 · 10.1097/01.mbc.0000245290.57021.46

  • Influence of the needle bore size on platelet count and routine coagulation testing

    Blood Coagulation & Fibrinolysis · 2006 · 10.1097/01.mbc.0000245300.10387.ca

  • An Epiisopicropodophyllin Aza Analogue via Palladium-Catalyzed Pseudo-Domino Cyclization

    The Journal of Organic Chemistry · 2002 · 10.1021/jo026068+

  • An Epiisopicropodophyllin Aza Analogue via Palladium-Catalyzed Pseudo-Domino Cyclization

    The Journal of Organic Chemistry · 2002 · 10.1021/jo026068+

  • Palladium in Organic Synthesis: Fundamental Transformations and Domino Processes

    Tetrahedron · 2000 · https://doi.org/10.1016/s0040-4020(00)00438-5

  • Asymmetric 1,4-additions of gilman reagents to α,β - disubstitoted (e)-enoylsultams / “enolate” protonations

    Tetrahedron · 1989 · 10.1016/0040-4020(89)80075-4

  • The osmylation of flexible 3-substituted cyclopentenes

    Tetrahedron Letters · 1989 · 10.1016/s0040-4039(00)70704-0

  • The osmylation of flexible 3-substituted cyclopentenes

    Tetrahedron Letters · 1989 · 10.1016/s0040-4039(00)70704-0

  • Asymmetric 1,4-additions of gilman reagents to α,β - disubstitoted (e)-enoylsultams / “enolate” protonations

    Tetrahedron · 1989 · 10.1016/0040-4020(89)80075-4

  • Norephedrine-derived 2-alkenyloxazolidines: stereochemistry of cyclization and allylic stereocenter directed asymmetric conjugate addition

    The Journal of Organic Chemistry · 1988 · 10.1021/jo00243a002

  • Stable and reactive conformations of N-enoyl-bornane-10.2-sultams in the absence of lewis acids : asymmetric 1.4-hydride additions

    Tetrahedron Letters · 1988 · 10.1016/0040-4039(88)85292-4

  • Stable and reactive conformations of N-enoyl-bornane-10.2-sultams in the absence of lewis acids : asymmetric 1.4-hydride additions

    Tetrahedron Letters · 1988 · 10.1016/0040-4039(88)85292-4

  • Enantioselective synthesis and absolute configuration of (−)-pulo'upone by asymmetric intramolecular diels-alder reaction

    Tetrahedron Letters · 1988 · 10.1016/s0040-4039(00)82216-9

  • Enantioselective synthesis and absolute configuration of (−)-pulo'upone by asymmetric intramolecular diels-alder reaction

    Tetrahedron Letters · 1988 · 10.1016/s0040-4039(00)82216-9

  • Norephedrine-derived 2-alkenyloxazolidines: stereochemistry of cyclization and allylic stereocenter directed asymmetric conjugate addition

    The Journal of Organic Chemistry · 1988 · 10.1021/jo00243a002

  • Asymmetric Induction at C(β) and C(α) of N‐Enoylsultams by Organomagnesium 1,4‐Addition/Enolate Trapping

    Helvetica Chimica Acta · 1987 · 10.1002/hlca.19870700825

  • Asymmetric Induction at C(β) and C(α) of N‐Enoylsultams by Organomagnesium 1,4‐Addition/Enolate Trapping

    Helvetica Chimica Acta · 1987 · 10.1002/hlca.19870700825

  • Asymmetric induction at C(β) and C(α) of N-enoyl sultams by 1,4-hydride addition/enolate trapping

    Tetrahedron Letters · 1986 · 10.1016/s0040-4039(00)85046-7

  • Asymmetric induction at C(β) and C(α) of N-enoyl sultams by 1,4-hydride addition/enolate trapping

    Tetrahedron Letters · 1986 · 10.1016/s0040-4039(00)85046-7

Current projects

    No projects listed.