Prof. Gérard BUONO
Prof.
Gérard
BUONO
AMU iSm2 AMU Case A62
Campus Scientifique de St Jérôme
13397
Marseille cedex 20
Phone number :
Fax :
0491 28 27 42
Publications (57)
Reference
Graphical abstract
HAL
Racemization mechanism of lithium tert ‐butylphenylphosphido‐borane: A kinetic insight
Rémy Fortrie, David Gatineau, Damien Hérault, Aurélie Béal, Jean‐valère Naubron, Laurent Giordano, Gérard Buono, Chirality, 2022, 34, 27-33. <hal-03632804>
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Introducing Chirality at Phosphorus Atoms: An Update on the Recent Synthetic Strategies for the Preparation of Optically Pure P-Stereogenic Molecules
Sébastien Lemouzy, Laurent Giordano, Damien Hérault, Gérard Buono, European Journal of Organic Chemistry, 2020, 2020, 3351 - 3366. <hal-03180299>
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Umpolung Reactivity of in Situ Generated Phosphido-Boranes: An Entry to P-Stereogenic Aminophosphine-Boranes
Sébastien Lemouzy, Romain Membrat, Enzo Olivieri, Marion Jean, Muriel Albalat, Didier Nuel, Laurent Giordano, Damien Hérault, Gérard Buono, Journal of Organic Chemistry, 2019, 4551-4557. <hal-02079962>
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Tunable P‐Stereogenic P,N‐Phosphine Ligands Design: Synthesis and Coordination Chemistry to Palladium
Sébastien Lemouzy, Marion Jean, Fabien Deplante, Muriel Albalat, Damien Hérault, Gérard Buono, ChemistrySelect, 2018, 3, 12281-12286. <hal-02079943>
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[2+1] Cycloaddition Affording Methylene-and Vinylidenecyclopropane Derivatives: A Journey around the Reactivity of Metal- Phosphinito-Phosphinous Acid Complexes
Hervé Clavier, Gérard Buono, Chemical Record, 2017, 17, 399-414. <hal-01591163>
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The hydroxyalkyl moiety as a protecting group for the stereospecific alkylation of masked secondary phosphine-boranes.
S. Lemouzy, M. Jean, L. Giordano, D. Hérault, G. Buono, Organic Letters, 18 (2016) 140-143. DOI: 10.1021/acs.orglett.5b03450
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Slowing down fat digestion and absorption by an oxadiazolone inhibitor targeting selectively gastric lipolysis
Vanessa Point, Anaïs Benarouche, Julie Zarrillo, Alexandre Guy, Romain Magnez, Laurence Fonseca, Brigitt Raux, Julien Leclaire, Gérard Buono, Frédéric Fotiadu, Thierry Durand, Frédéric Carrière, Carole Vaysse, Leslie Couedelo, Jean-François Cavalier, European Journal of Medicinal Chemistry, 2016, 123. <hal-01466841>
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[RuCl2(η6-p-cymene)] complexes bearing phosphinous acid ligands: preparation, application in C–H bond functionalization and mechanistic investigations
Lionel Graux, Michel Giorgi, Gérard Buono, Hervé Clavier, Dalton Transactions, 2016. <hal-01409748>
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Mechanistic aspects of the stereospecific reduction of chiral hydroxyalkyl phosphinates and phosphine oxides
Sébastien Lemouzy, Duc-Hanh Nguyen, David Gatineau, Laurent Giordano, Damien Hérault, Gérard Buono, Pure and Applied Chemistry, 2016. <hal-01439393>
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The Hydroxyalkyl Moiety As a Protecting Group for the Stereospeci c Alkylation of Masked Secondary Phosphine-Boranes
Sébastien Lemouzy, Marion Jean, Laurent Giordano, Damien Hérault, Gérard Buono, Organic Letters, 2016. <hal-01439387>
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Pages
| Reference | Graphical abstract | HAL |
|---|---|---|
|
Racemization mechanism of lithium tert ‐butylphenylphosphido‐borane: A kinetic insight |
|
✖ |
|
Introducing Chirality at Phosphorus Atoms: An Update on the Recent Synthetic Strategies for the Preparation of Optically Pure P-Stereogenic Molecules |
|
✓ |
|
Umpolung Reactivity of in Situ Generated Phosphido-Boranes: An Entry to P-Stereogenic Aminophosphine-Boranes |
|
✓ |
|
Tunable P‐Stereogenic P,N‐Phosphine Ligands Design: Synthesis and Coordination Chemistry to Palladium |
|
✓ |
|
[2+1] Cycloaddition Affording Methylene-and Vinylidenecyclopropane Derivatives: A Journey around the Reactivity of Metal- Phosphinito-Phosphinous Acid Complexes |
|
✓ |
|
The hydroxyalkyl moiety as a protecting group for the stereospecific alkylation of masked secondary phosphine-boranes. |
|
✖ |
|
Slowing down fat digestion and absorption by an oxadiazolone inhibitor targeting selectively gastric lipolysis |
|
✖ |
|
[RuCl2(η6-p-cymene)] complexes bearing phosphinous acid ligands: preparation, application in C–H bond functionalization and mechanistic investigations |
|
✓ |
|
Mechanistic aspects of the stereospecific reduction of chiral hydroxyalkyl phosphinates and phosphine oxides |
|
✖ |
|
The Hydroxyalkyl Moiety As a Protecting Group for the Stereospeci c Alkylation of Masked Secondary Phosphine-Boranes |
|
✖ |