P. Dauban

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Nitrene chemistry in organic synthesis: still in its infancy?

Valérie Pons, Geoffroy Dequirez, P. Dauban, 2012, Angewandte Chemie.

The expression and function of Ca2+‐sensing receptors in rat mesenteric artery; comparative studies using a model of type II diabetes

D. Ward, P. Dauban, G. Edwards, 2008, British journal of pharmacology.

A masked 1,3-dipole revealed from aziridines.

P. Dauban, G. Malik, 2009, Angewandte Chemie.

Modeling and Mutagenesis of the Binding Site of Calhex 231, a Novel Negative Allosteric Modulator of the Extracellular Ca2+-sensing Receptor*

D. Rognan, P. Dauban, Albane Kessler, 2003, Journal of Biological Chemistry.

Calindol, a Positive Allosteric Modulator of the Human Ca2+ Receptor, Activates an Extracellular Ligand-binding Domain-deleted Rhodopsin-like Seven-transmembrane Structure in the Absence of Ca2+*

P. Dauban, J. Northup, M. Ruat, 2005, Journal of Biological Chemistry.

Positive and Negative Allosteric Modulators of the Ca2+-sensing Receptor Interact within Overlapping but Not Identical Binding Sites in the Transmembrane Domain*

Didier Rognan, D. Rognan, P. Dauban, 2004, Journal of Biological Chemistry.

Design and synthesis of cyclic sulfonamides and sulfamates as new calcium sensing receptor agonists.

T. Gorojankina, P. Dauban, M. Ruat, 2010, Bioorganic & medicinal chemistry letters.

Molecular determinants of allosteric modulators of the calcium-sensing receptor

D. Rognan, P. Dauban, Albane Kessler, 2006, Journal of Physiology-Paris.

Evidence in Favor of a Calcium-Sensing Receptor in Arterial Endothelial Cells: Studies With Calindol and Calhex 231

J. Ohanian, D. Ward, P. Dauban, 2005, Circulation research.

N2-benzyl-N1-(1-(1-naphthyl)ethyl)-3-phenylpropane-1,2-diamines and conformationally restrained indole analogues: development of calindol as a new calcimimetic acting at the calcium sensing receptor.

P. Dauban, Albane Kessler, M. Ruat, 2004, Bioorganic & medicinal chemistry letters.

N1-Arylsulfonyl-N2-(1-aryl)ethyl-3-phenylpropane-1,2-diamines as novel calcimimetics acting on the calcium sensing receptor.

P. Dauban, M. Ruat, H. Faure, 2000, Bioorganic & medicinal chemistry letters.

7.19 Addition Reactions with Formation of Carbon Nitrogen Bonds

P. Dauban, B. Darses, Amanda G. Jarvis, 2014 .

Rhodium-Catalyzed Alkene Difunctionalization with Nitrenes.

Geoffroy Dequirez, P. Dauban, P. Retailleau, 2016, Chemistry.

Regioselective access to substituted oxindoles via rhodium-catalyzed carbene C–H insertion

P. Dauban, R. Dodd, D. Gauthier, 2009 .

Two enantiomerically pure cyclic arenesulfonamide hydrochloride salts.

P. Dauban, P. Retailleau, R. Dodd, 2009, Acta crystallographica. Section C, Crystal structure communications.

N1‐Arylsulfonyl‐N2‐(1‐(1‐naphthyl)ethyl)‐1,2‐diaminocyclohexanes: A New Class of Calcilytic Agents Acting at the Calcium‐Sensing Receptor

P. Dauban, Albane Kessler, M. Ruat, 2004 .

New C5-alkylated indolobenzazepinones acting as inhibitors of tubulin polymerization: cytotoxic and antitumor activities.

J. Wdzieczak‐Bakala, J. Bignon, P. Dauban, 2008, Journal of medicinal chemistry.

Copper‐Promoted Tandem Three‐Component Access to Quinazolin‐4(H)‐imines and Benzimidazo[1,2‐c]quinazolines

R. Rodrigues, P. Dauban, L. Neuville, 2019, Advanced Synthesis & Catalysis.

Catalytic C-H amination: recent progress and future directions.

P. Dauban, F. Collet, R. Dodd, 2009, Chemical communications.

Late-stage C-H amination of abietane diterpenoids.

P. Dauban, P. H. Di Chenna, B. Darses, 2019, Organic & biomolecular chemistry.

Asymmetric Synthesis of Enantiopure Pyrrolidines by C(sp 3 )−H Amination of Hydrocarbons

P. Dauban, P. Retailleau, T. Saget, 2021, Angewandte Chemie.

Asymmetric Synthesis of Enantiopure Pyrrolidines by C(sp3)-H Amination of Hydrocarbons.

P. Dauban, P. Retailleau, T. Saget, 2021, Angewandte Chemie.

Catalytic Intermolecular C(sp3)–H Amination with Sulfamates for the Asymmetric Synthesis of Amines

P. Dauban, B. Darses, Yanis Lazib, 2020 .

Catalytic Enantioselective Intermolecular Benzylic C(sp3 )-H Amination.

P. Dauban, P. Retailleau, B. Darses, 2019, Angewandte Chemie.

Catalytic Enantioselective Intermolecular Benzylic C(sp 3 )−H Amination

P. Dauban, P. Retailleau, B. Darses, 2019, Angewandte Chemie.

Catalytic Intramolecular C(sp3)-H Amination of Carbamimidates

P. Dauban, P. Retailleau, G. Grelier, 2017 .

Dirhodium(II)-Mediated Alkene Epoxidation with Iodine(III) Oxidants

P. Dauban, G. Grelier, B. Darses, 2018, European Journal of Organic Chemistry.

Synthesis and GABA(A) receptor activity of 2,19-sulfamoyl analogues of allopregnanolone.

P. Dauban, G. Burton, R. Dodd, 2009, Bioorganic & medicinal chemistry.

PhINSes mediated aziridination of 11-pregnane derivatives: synthesis of an 11,12-aziridino analogue of neuroactive steroids

P. Dauban, M. Garland, R. Baggio, 2003 .

Aziridination of 11-pregnene-3,20-dione using PhIN-Ses

P. Dauban, G. Burton, P. Chenna, 2000 .

Catalytic C-H amination: the stereoselectivity issue.

P. Dauban, F. Collet, C. Lescot, 2011, Chemical Society reviews.

Iminoiodane mediated aziridination of α-allylglycine: access to a novel rigid arginine derivative and to the natural amino acid enduracididine

J. Bourguignon, P. Dauban, R. Dodd, 2004 .

Intramolecular PhI=O mediated copper-catalyzed aziridination of unsaturated sulfamates: a new direct access to polysubstituted amines from simple homoallylic alcohols.

P. Dauban, G. Burton, R. Dodd, 2002, Organic letters.

Intermolecular C-H amination of complex molecules: insights into the factors governing the selectivity.

P. Dauban, P. Retailleau, F. Collet, 2012, The Journal of organic chemistry.

Intramolecular bromine-catalyzed aziridination: a new direct access to cyclic sulfonamides

P. Dauban, R. Dodd, 2001 .

Catalytic Intermolecular C(sp3)-H Amination: Selective Functionalization of Tertiary C-H Bonds vs Activated Benzylic C-H Bonds.

P. Dauban, T. Saget, E. Van Elslande, 2021, Journal of the American Chemical Society.

N(1)-Arylsulfonyl-N(2)-(1-(1-naphthyl)ethyl)-1,2-diaminocyclohexanes: a new class of calcilytic agents acting at the calcium-sensing receptor.

P. Dauban, Albane Kessler, M. Ruat, 2004, Chembiochem : a European journal of chemical biology.

Hypervalent organoiodine compounds: from reagents to valuable building blocks in synthesis

P. Dauban, G. Grelier, B. Darses, 2018, Beilstein journal of organic chemistry.

Copper-catalyzed nitrogen transfer mediated by iodosylbenzene PhI=O.

P. Dauban, R. Dodd, L. Sanière, 2001, Journal of the American Chemical Society.

PhI[Formula: see text]NSes: A New Iminoiodinane Reagent for the Copper-Catalyzed Aziridination of Olefins.

P. Dauban, R. Dodd, 1999, The Journal of organic chemistry.

Synthesis of Indolobenzazepinones by Application of an Isocyanide‐Based Multicomponent Reaction

P. Dauban, P. Retailleau, R. Dodd, 2008 .

The Multiple Facets of Iodine(III) Compounds in an Unprecedented Catalytic Auto-amination for Chiral Amine Synthesis.

P. Dauban, F. Taran, G. Grelier, 2016, Angewandte Chemie.

Tandem Catalytic C(sp(3) )-H Amination/Sila-Sonogashira-Hagihara Coupling Reactions with Iodine Reagents.

P. Dauban, B. Darses, Julien Buendia, 2015, Angewandte Chemie.

Bis(2,2‐dimethylpropanoato ‐ κ‐O)phenyl‐iodine

Valérie Pons, Geoffroy Dequirez, P. Dauban, 2013 .

Synthesis of cyclic sulfonamides via intramolecular copper-catalyzed reaction of unsaturated iminoiodinanes.

P. Dauban, R. Dodd, 2000, Organic letters.

N1-Benzoyl-N2-[1-(1-naphthyl)ethyl]-trans-1,2-diaminocyclohexanes: Development of 4-chlorophenylcarboxamide (calhex 231) as a new calcium sensing receptor ligand demonstrating potent calcilytic activity.

D. Rognan, P. Dauban, Albane Kessler, 2006, Journal of medicinal chemistry.

Regioselective electrophilic substitution of 2,3-aziridino-γ-lactones: preliminary studies aimed at the synthesis of α,α-disubstituted α- or β-amino acids

P. Dauban, R. Dodd, M. S. Valle, 2008 .

Intermolecular Alkene Aziridination: An Original and Efficient CuI···CuI Dinuclear Catalyst Deriving from a Phospha‐Amidinate Ligand

P. Dauban, D. Bourissou, B. Martín-Vaca, 2013 .

Efficient diastereoselective intermolecular rhodium-catalyzed C-H amination.

P. Müller, Corinne Fruit, P. Dauban, 2006, Angewandte Chemie.

Sulfonimidamides: efficient chiral iminoiodane precursors for diastereoselective copper-catalyzed aziridination of olefins.

P. Dauban, F. Robert-Peillard, P. H. Di Chenna, 2004, Organic letters.

Transition metal-catalyzed iodine(iii)-mediated nitrene transfer reactions: efficient tools for challenging syntheses.

R. Rodrigues, P. Dauban, L. Neuville, 2017, Chemical communications.

Dirhodium(II)-Catalyzed C(sp3)–H Amination Using Iodine(III) Oxidants

P. Dauban, G. Grelier, Julien Buendia, 2015 .

Catalytic oxyamidation of indoles.

Valérie Pons, P. Dauban, P. Retailleau, 2010, Angewandte Chemie.

Studies on the formal [3 + 2] cycloaddition of aziridines with alkenes for the synthesis of 1-azaspiroalkanes.

P. Fleurat‐Lessard, P. Dauban, P. Retailleau, 2015, The Journal of organic chemistry.

Rh‐, Ag‐, and Cu‐Catalyzed C–N Bond Formation

M. M. Díaz‐Requejo, P. Pérez, P. Dauban, 2012 .

Catalytic intermolecular alkene oxyamination with nitrenes.

Geoffroy Dequirez, P. Dauban, P. Retailleau, 2014, Chemistry.

Asymmetric Synthesis of Amines through Rhodium-Catalyzed C-H Amination with Sulfonimidoylnitrenes

P. Dauban, B. Darses, Amanda G. Jarvis, 2013 .

Catalytic C–H amination of alkanes with sulfonimidamides: silver(I)-scorpionates vs. dirhodium(II) carboxylates

M. M. Díaz‐Requejo, P. Pérez, P. Dauban, 2013 .

Catalytic stereoselective alkene aziridination with sulfonimidamides

P. Dauban, F. Robert-Peillard, F. Collet, 2010 .

Toward a synthetically useful stereoselective C-H amination of hydrocarbons.

P. Müller, P. Dauban, F. Robert-Peillard, 2008, Journal of the American Chemical Society.

Diastereoselective rhodium-catalyzed nitrene transfer starting from chiral sulfonimidamide-derived iminoiodanes

G. Bernardinelli, P. Müller, Corinne Fruit, 2005 .

First enantiospecific synthesis of a 3,4-dihydroxy-L-glutamic acid [(3S,4S)-DHGA], a new mGluR1 agonist.

L. Prézeau, J. Pin, F. Acher, 2000, Bioorganic & medicinal chemistry letters.

Application of 2,3-aziridino-γ-lactone methodology toward the enantiospecific synthesis of the (3S,4S)-isomer of dihydroxy-L-glutamic acid

P. Dauban, R. Dodd, Carole de Saint-Fuscien, 1999 .

Reaction of Ynamides with Iminoiodinane-Derived Nitrenes: Formation of Oxazolones and Polyfunctionalized Oxazolidinones.

P. Dauban, P. Retailleau, G. Grelier, 2017, The Journal of organic chemistry.

Enantiospecific Synthesis of a Protected Equivalent of APTO, the β-Amino Acid Fragment of Microsclerodermins C and D, by Aziridino-γ-lactone Methodology

P. Dauban, R. Dodd, M. S. Valle, 2009 .

Regioselective Electrophilic Substitution of 2,3-Aziridino-γ-lactones: Preliminary Studies Aimed at the Synthesis of α,α-Disubstituted α- or β-Amino Acids.

P. Dauban, R. Dodd, M. S. Valle, 2008 .

Enantiospecific total synthesis of (-)-polyoxamic acid using 2,3-aziridino-gamma-lactone methodology.

P. Dauban, R. Dodd, Aurélie Tarrade, 2003, The Journal of organic chemistry.

A new straightforward synthesis of 2,3-aziridino-γ-lactones

P. Dauban, R. Dodd, Carole de Saint-Fuscien, 2000 .

2,3-Aziridino-2,3-dideoxy-D-ribono-gamma-lactone 5-Phosphonate: Stereocontrolled Synthesis from D-Lyxose and Unusual Aziridine Ring Opening.

P. Dauban, R. Dodd, 1997, The Journal of organic chemistry.

Synthesis of Optically Pure 3,4-Disubstituted l-Glutamates from a Novel 2,3-Aziridino-γ-lactone 4-Carboxylate Derivative

P. Dauban, A. Chiaroni, R. Dodd, 1996 .

Reactivity of 2,3-Aziridino-2,3-dideoxy-D-lyxono-.gamma.-lactone Derivatives, Rigid Analogs of Aziridine-2-carboxylic Esters, toward Soft and Hard Nucleophiles: Control of Lactone vs Aziridine Ring Opening and C-2 vs C-3 Regioselectivity

P. Dauban, M. T. H. Dau, R. Dodd, 1995 .

Catalytic C-H amination: a reaction now accessible to engineered natural enzymes.

J. Mahy, P. Dauban, Jennifer Ciesielski, 2014, Angewandte Chemie.

A Short Asymmetric Synthesis of Octahydroindole Derivatives by Application of Catalytic C(sp3)–H Amination Reaction

P. Dauban, P. Retailleau, C. Lescot, 2014 .

Catalytic selective oxyamidation of cyclic enamides using nitrenes.

Geoffroy Dequirez, P. Dauban, P. Retailleau, 2012, Chemistry.

Iminoiodanes and C-NBond Formation in Organic Synthesis

P. Dauban, R. Dodd, 2003 .

[N‐(2‐(Trimethylsilyl)ethanesulfonyl)imino]phenyliodane

P. Dauban, R. Dodd, 2003 .

Stereoselective C  N Bond‐Forming Reactions Through C ( sp 3

P. Dauban, Romain Rey-Rodriguez, Ali Nasrallah, 2019, C‐H Activation for Asymmetric Synthesis.

Studies in catalytic C-H amination involving nitrene C-H insertion.

P. Dauban, F. Collet, C. Lescot, 2010, Dalton transactions.

Intermolecular Rhodium(II)-Catalyzed Allylic C(sp 3)-H Amination of Cyclic Enamides

P. Dauban, P. Retailleau, V. Gandon, 2018 .

Synthesis of 2,3-aziridino-2,3-dideoxy-D-lyxono-γ-lactone 5-phosphonate from D-ribose, a new member of the 2,3-aziridino-γ-lactone family of synthons

P. Dauban, R. Dodd, B. Hofmann, 1997 .

Aziridines from intramolecular alkene aziridination of sulfamates: reactivity toward carbon nucleophiles. application to the synthesis of spisulosine and its fluoro analogue.

P. Dauban, P. Retailleau, G. Malik, 2011, The Journal of organic chemistry.

Enantiospecific synthesis of 3,4-disubstituted glutamic acids via controlled stepwise ring-opening of 2,3-aziridino-γ-lactone

P. Dauban, Zhaohua Yan, R. Dodd, 2002 .

Synthesis of 2,3-Aziridino-2,3-dideoxy-D-lyxono-γ-lactone 5- Phosphonate from D-Ribose, a New Member of the 2,3-Aziridino-γ- lactone Family of Synthons.

P. Dauban, R. Dodd, B. Hofmann, 1997 .

Approach to pactamycin analogues using rhodium(II)-catalyzed alkene aziridination and C(sp3)–H amination reactions

R. Rodrigues, P. Dauban, L. Neuville, 2018 .

Application of the Evans aziridination procedure to 2-substituted acrylates and cinnamates: An expedient route to α-substituted α- and β-amino acids

P. Dauban, R. Dodd, 1998 .

Evidence for the presence of GPRC6A receptors in rat mesenteric arteries.

D. Ward, P. Dauban, G. Edwards, 2008, Cell calcium.

Light‐Induced Activation of the Du Bois [RhII2(Esp)2] Catalyst for Nitrogen Atom Transfer Reactions

P. Dauban, A. Aukauloo, R. Guillot, 2017 .

Application of the Evans Aziridination Procedure to 2-Substituted Acrylates and Cinnamates: An Expedient Route to α-Substituted α- and β-Amino Acids.

P. Dauban, R. Dodd, 1998 .

Rhodium(II)-Catalyzed Enantioselective Intermolecular Aziridination of Alkenes.

P. Dauban, P. Retailleau, P. H. Di Chenna, 2022, Journal of the American Chemical Society.

Total synthesis and absolute configuration of the natural amino acid tetrahydrolathyrine.

S. H. Cardoso, P. Dauban, P. Retailleau, 2009, The Journal of organic chemistry.

Copper‐Catalyzed Nitrogen Transfer Mediated by Iodosylbenzene PhI=O.

P. Dauban, R. Dodd, L. Sanière, 2001 .

PhI=NSes: A New Iminoiodinane Reagent for the Copper‐Catalyzed Aziridination of Olefins.

P. Dauban, R. Dodd, 1999 .

Synthesis of 6,19-sulfamidate bridged pregnanes.

P. Dauban, G. Burton, R. Dodd, 2005, The Journal of organic chemistry.

One-pot double Suzuki-Miyaura couplings: rapid access to nonsymmetrical tri(hetero)aryl derivatives.

P. Dauban, R. Dodd, F. Beaumard, 2009, Organic letters.

Stereoselective rhodium-catalyzed imination of sulfides.

P. Dauban, F. Collet, R. Dodd, 2008, Organic letters.

Late‐stage Rh(II)‐catalyzed Nitrene Transfer for the Synthesis of Guaianolide Analogs with Enhanced Antiproliferative Activity

P. Dauban, J. Padrón, Viviana E. Nicotra, 2021 .

Presynaptic External Calcium Signaling Involves the Calcium-Sensing Receptor in Neocortical Nerve Terminals

P. Dauban, M. Ruat, Stephen M. Smith, 2010, PloS one.

Molecular determinants of non-competitive antagonist binding to the mouse GPRC6A receptor.

D. Rognan, T. Gorojankina, P. Dauban, 2009, Cell calcium.

Asymmetric Intramolecular Buchner Reaction: From High Stereoselectivity to Coexistence of Norcaradiene, Cycloheptatriene, and an Intermediate Form in the Solid State.

P. Maldivi, C. Philouze, J. Poisson, 2021, Organic letters.

Redox-responsive catalysis: fine tuning of chemoselectivity in the intramolecular reaction of diazo compounds catalysed by ferrocene-functionalised dirhodium(ii) complexes

P. Dauban, R. Poli, E. Manoury, 2023, New Journal of Chemistry.

Optimized Conditions for Passerini-Smiles Reactions and Applications to Benzoxazinone Syntheses

P. Dauban, P. Retailleau, Laurent El Kaïm, 2016, Molecules.

Iminoiodanes and C—N Bond Formation in Organic Synthesis

P. Dauban, R. Dodd, 2003 .

The expression and function of Ca(2+)-sensing receptors in rat mesenteric artery; comparative studies using a model of type II diabetes.

D. Ward, P. Dauban, G. Edwards, 2008 .

Asymmetric Syntheses of Enantioenriched 2,5-Disubstituted Pyrrolidines

P. Dauban, T. Saget, A. Labande, 2023, ACS organic & inorganic Au.

Photocatalytic C−H Functionalization of Nitrogen Heterocycles Mediated by a Redox Active Protecting Group

P. Dauban, E. G. Mata, T. Saget, 2023, European Journal of Organic Chemistry.

Catalyst-Controlled Intermolecular Homobenzylic C(sp3)-H Amination for the Synthesis of β-Arylethylamines.

P. Dauban, E. D. Sosa Carrizo, Vincent Boquet, 2024, Journal of the American Chemical Society.

Copper-catalyzed aziridination of allylglycine derivatives

P. Dauban, R. Dodd, L. Sanière, 2003 .