Giovanni Poli
Researcher Next ID · RN-041109
Researcher · Chemistry
Centre National de la Recherche Scientifique
Paris, Portugal
- Works count
- 394
- Citation count
- 6,515
- H-index
- 40
- i10-index
- 155
Research interests
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
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