المؤلفون: Erwan Brunard, Vincent Boquet, Tanguy Saget, E. Daiann Sosa Carrizo, Marie Sircoglou, Philippe Dauban

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Biotechnology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, selective intermolecular amination, energy decomposition analysis, computational investigations evidenced, asynchronous transition state, homobenzylic position due, unactivated homobenzylic c, β ‑ arylethylamines, c <, utmost interest, thereby providing, tetracarboxylate allows, tailored sulfamate, rely mainly, orbital interaction, medicinal chemistry, high level, direct access, concerted mechanism, catalytic pocket, benzylic ratio

Relation: https://figshare.com/articles/journal_contribution/Catalyst-Controlled_Intermolecular_Homobenzylic_C_sp_sup_3_sup_H_Amination_for_the_Synthesis_of_Arylethylamines/25270554

الاتاحة: https://doi.org/10.1021/jacs.3c10964.s002
https://figshare.com/articles/journal_contribution/Catalyst-Controlled_Intermolecular_Homobenzylic_C_sp_sup_3_sup_H_Amination_for_the_Synthesis_of_Arylethylamines/25270554

المؤلفون: Erwan Brunard (10702269), Vincent Boquet (8114546), Elsa Van Elslande (8179908), Tanguy Saget (1981075), Philippe Dauban (255170)

مصطلحات موضوعية: Biophysics, Biochemistry, Evolutionary Biology, Immunology, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Catalytic, TBPhsNH, combination, Rh 2, substrate, yield, tert, Intermolecular, bond, functionalized, BDE, benzylic site, Activated, NH, 0.01, rhodium-bound nitrene species, amines, tfpttl, site-selectivity results, catalyst, butylphenol sulfamate, amide, 50 mmol scale

Relation: https://figshare.com/articles/journal_contribution/Catalytic_Intermolecular_C_sp_sup_3_sup_H_Amination_Selective_Functionalization_of_Tertiary_C_H_Bonds_vs_Activated_Benzylic_C_H_Bonds/14488881

الاتاحة: https://doi.org/10.1021/jacs.1c03872.s001

المؤلفون: Gwendal Grelier, Benjamin Darses, Philippe Dauban

المصدر: Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1508-1528 (2018)

مصطلحات موضوعية: atom-economy, couplings, hypervalent iodine, oxidation, tandem reactions, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/88af3c22266f4b22a799a99567bdf127

المؤلفون: Yanis Lazib, Junio Guimaraes Naves, Agnès Labande, Philippe Dauban, Tanguy Saget

المصدر: ACS Organic & Inorganic Au.

مصطلحات موضوعية: Cultural Studies, History, Literature and Literary Theory

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f4ef30a8cd699368affa676aba4cda7c
https://doi.org/10.1021/acsorginorgau.2c00061

المؤلفون: Illia Ruzhylo, Sandrine Vincendeau, Philippe Dauban, Eric Manoury, Rinaldo Poli, Agnès Labande

المساهمون: Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Institut Universitaire de France (IUF), Ministère de l'Education nationale, de l’Enseignement supérieur et de la Recherche (M.E.N.E.S.R.), ANR-19-CE07-0043,CHamRhOx,Modulation rédox d'insertions de nitrènes dans des liaisons C(sp3)-H catalysées au rhodium(2019)

المصدر: New Journal of Chemistry
New Journal of Chemistry, 2023, 47 (20), pp.9601-9610. ⟨10.1039/D3NJ01131C⟩

مصطلحات موضوعية: [CHIM.ORGA]Chemical Sciences/Organic chemistry, Materials Chemistry, General Chemistry, [CHIM.CATA]Chemical Sciences/Catalysis, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4db098c2eef830de5a7e743993ecab7
https://hal.science/hal-04099187

المؤلفون: Vincent Boquet, Ali Nasrallah, Alejandro L. Dana, Erwan Brunard, Pablo H. Di Chenna, Fernando J. Duran, Pascal Retailleau, Benjamin Darses, Marie Sircoglou, Philippe Dauban

المصدر: Journal of the American Chemical Society. 144(37)

مصطلحات موضوعية: Colloid and Surface Chemistry, Aziridines, Rhodium, Stereoisomerism, General Chemistry, Alkenes, Biochemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6390efa1b54f3c769fb7a6116c387156
https://pubmed.ncbi.nlm.nih.gov/36094904

المؤلفون: Yanis Lazib, Benjamin Darses, Tanguy Saget, Pascal Retailleau, Philippe Dauban

المصدر: Angewandte Chemie International Edition. 60:21708-21712

مصطلحات موضوعية: chemistry.chemical_compound, Enantiopure drug, Stereochemistry, Chemistry, Nitrene, Enantioselective synthesis, Stereoselectivity, General Chemistry, Catalysis, Amination, Pyrrolidine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3d081cf50ab1d2715965c3711fd58e50
https://doi.org/10.1002/anie.202107898

المؤلفون: Philippe Dauban, Erwan Brunard, Elsa Van Elslande, Tanguy Saget, Vincent Boquet

المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)

المصدر: Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2021, 143 (17), pp.6407-6412. ⟨10.1021/jacs.1c03872⟩

مصطلحات موضوعية: [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Chemistry, digestive, oral, and skin physiology, Intermolecular force, [CHIM.CATA]Chemical Sciences/Catalysis, General Chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, Medicinal chemistry, Catalysis, 0104 chemical sciences, Colloid and Surface Chemistry, Surface modification, Amination

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723a6ab570fbe1e293792fd55ee77bad
https://doi.org/10.1021/jacs.1c03872

المؤلفون: Philippe Dauban, Tanguy Saget

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e5f5bd5174509642488948a93b0fa944
https://doi.org/10.1142/9789811248436_0008

المؤلفون: Philippe Dauban, Viviana E. Nicotra, Benjamin Darses, José M. Padrón, Sebastián J Castro

المساهمون: Consejo Nacional de Investigaciones Científicas y Técnicas, Instituto Multidisciplinario de Biología Vegetal (IMBIV), and Factulad de Ciencias Exactas, Físicas y Naturales, Universidad Nacional de Córdoba, Córdoba, Argentina, Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Univ. Grenoble Alpes, CNRS, DCM, 38000 Grenoble, France

المصدر: European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (12), pp.1859-1863. ⟨10.1002/ejoc.202100074⟩
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET

مصطلحات موضوعية: C−H AMINATION, Reaction conditions, chemistry.chemical_classification, ANTIPROLIFERATIVE ACTIVITY, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Chemistry, Alkene, Stereochemistry, Nitrene, Organic Chemistry, Late stage, Biological activity, 010402 general chemistry, 01 natural sciences, 0104 chemical sciences, Catalysis, purl.org/becyt/ford/1 [https], LATE-STAGE FUNCTIONALIZATION, NITRENES, purl.org/becyt/ford/1.4 [https], Physical and Theoretical Chemistry, Solid tumor, Amination, SESQUITERPENES

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27617c7d421a19843e9003dc6838879f
https://doi.org/10.1002/ejoc.202100074

المؤلفون: Elodie Martinand-Lurin, Aurélie Dos Santos, Emmanuelle Robineau, Pascal Retailleau, Philippe Dauban, Laurence Grimaud, Laurent El Kaïm

المصدر: Molecules; Volume 21; Issue 9; Pages: 1257

مصطلحات موضوعية: isocyanide, Passerini-Smiles, multicomponent reaction, heterocycles, benzoxazinones

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules21091257

الاتاحة: https://doi.org/10.3390/molecules21091257

المؤلفون: Loic Leman, Laurent Saniere, Philippe Dauban, Robert H. Dodd

المصدر: ARKIVOC, Vol 2003, Iss 6, Pp 126-134 (2003)

مصطلحات موضوعية: Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0004.615; https://doaj.org/toc/1551-7004; https://doaj.org/toc/1551-7012

URL الوصول: https://doaj.org/article/0dfe188dea9e45cc90e2ba3b9408c9f9

المؤلفون: Vincent Boquet, Philippe Dauban, Benjamin Darses, Ali Nasrallah, Yanis Lazib

المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)

المصدر: Organic Process Research and Development
Organic Process Research and Development, American Chemical Society, 2019, 24 (5), pp.724-728. ⟨10.1021/acs.oprd.9b00424⟩

مصطلحات موضوعية: [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Nitrene, Organic Chemistry, Intermolecular force, Enantioselective synthesis, chemistry.chemical_element, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, 01 natural sciences, 0104 chemical sciences, Rhodium, Catalysis, chemistry.chemical_compound, chemistry, Carbon–nitrogen bond, Polymer chemistry, Physical and Theoretical Chemistry, ComputingMilieux_MISCELLANEOUS, Amination

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d96bc700c8a9fc18a113c90cf6e57ab
https://doi.org/10.1021/acs.oprd.9b00424

المؤلفون: Ali Nasrallah, Romain Rey-Rodriguez, Philippe Dauban

المصدر: C-H Activation for Asymmetric Synthesis

مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Hydrogen bond, Nitrene, Bond, chemistry.chemical_element, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, 0104 chemical sciences, Rhodium, Catalysis, Metal, chemistry.chemical_compound, visual_art, visual_art.visual_art_medium, Stereoselectivity, Azide

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::af4405e2fcc6f8b21458606097c0dd90
https://doi.org/10.1002/9783527810857.ch2

المؤلفون: Ali Nasrallah, Vincent Boquet, Alexandra Hecker, Pascal Retailleau, Benjamin Darses, Philippe Dauban

المصدر: Angewandte Chemie. 131:8276-8280

مصطلحات موضوعية: General Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::ed5821f14254a7d6161133da7f347473
https://doi.org/10.1002/ange.201902882

المؤلفون: Philippe, Dauban, Robert H, Dodd

المصدر: The Journal of organic chemistry. 64(14)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::e1f2dfb51b00d483d52f63c8d7d1f439
https://pubmed.ncbi.nlm.nih.gov/34237848

المؤلفون: Erwan, Brunard, Vincent, Boquet, Elsa, Van Elslande, Tanguy, Saget, Philippe, Dauban

المصدر: Journal of the American Chemical Society. 143(17)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::5ecb3bea052750ece4231900cd93948d
https://pubmed.ncbi.nlm.nih.gov/33900759

المؤلفون: Christian Philouze, Pascale Maldivi, Jean-François Poisson, Philippe Dauban, Benjamin Darses

المساهمون: Département de Chimie Moléculaire (DCM), Université Grenoble Alpes (UGA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Institut de Recherche Interdisciplinaire de Grenoble (IRIG), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA), ANR-17-EURE-0003,CBH-EUR-GS,CBH-EUR-GS(2017)

المصدر: Organic Letters
Organic Letters, American Chemical Society, 2021, 23 (2), pp.300-304. ⟨10.1021/acs.orglett.0c03774⟩
Organic Letters, 2021, 23 (2), pp.300-304. ⟨10.1021/acs.orglett.0c03774⟩

مصطلحات موضوعية: Valence (chemistry), Bicyclic molecule, 010405 organic chemistry, Chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, Absolute configuration, Cycloheptatriene, Crystal structure, 010402 general chemistry, 01 natural sciences, Biochemistry, 0104 chemical sciences, Stereocenter, Crystallography, chemistry.chemical_compound, Intramolecular force, [CHIM.CRIS]Chemical Sciences/Cristallography, Stereoselectivity, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fa9fcdbca3beb26ecb1020b9c4eb106
https://hal.archives-ouvertes.fr/hal-03371078/document

المؤلفون: María Ivana Lapuh, Philippe Dauban, Ali Nasrallah, Fernando Javier Duran, Gwendal Grelier, Benjamin Darses

المصدر: European Journal of Organic Chemistry. 2018:5836-5842

مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Nitrene, Organic Chemistry, chemistry.chemical_element, Alkene epoxidation, 010402 general chemistry, Iodine, 01 natural sciences, Medicinal chemistry, 0104 chemical sciences, Rhodium, Reagent, Oxidizing agent, Lewis acids and bases, Physical and Theoretical Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::35a066144c76e6dd5fd2a97e1105c6a3
https://doi.org/10.1002/ejoc.201800306

المؤلفون: Philippe Dauban, Gwendal Grelier, Benjamin Darses

المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Département de Chimie Moléculaire (DCM), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019])

المصدر: Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1508-1528 (2018)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Beilstein-Institut, 2018, 14, pp.1508-1528. ⟨10.3762/bjoc.14.128⟩

مصطلحات موضوعية: oxidation, Review, 010402 general chemistry, 01 natural sciences, Coupling reaction, Catalysis, lcsh:QD241-441, chemistry.chemical_compound, lcsh:Organic chemistry, Atom economy, tandem reactions, lcsh:Science, Nucleophilic addition, atom-economy, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Aryl, couplings, Organic Chemistry, Hypervalent molecule, Combinatorial chemistry, 0104 chemical sciences, Chemistry, hypervalent iodine, chemistry, Reagent, lcsh:Q, Stoichiometry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b72715d9c281d13a516aeb4f560d8e3
https://doaj.org/article/88af3c22266f4b22a799a99567bdf127