Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Gérard Guillamot"'
Autor:
Jean-Pierre Armand, Marie-Priscille Brun, Janine Cossy, Joël Doré, Philippe Duchateau, Gérard Guillamot, Jean-François Haeuw, Patricia Melnyk, Alexandre Pachot, Sophie Postel-Vinay, Raphaël Rodriguez, Nathalie Strub-Wourgaft, Bruno Villoutreix, Bernard Meunier
Acteurs ou bénéficiaires, nous sommes tous spectateurs sidérés de l'ampleur des progrès de la médecine. Ils sont la conséquence des découvertes du XXe siècle, en particulier sur la biologie moléculaire et le génome. La recherche du XXIe si
Autor:
Kevin Simon, Desiree Znidar, Julien Boutet, Gérard Guillamot, Jean-Yves Lenoir, Doris Dallinger, C. Oliver Kappe
Publikováno v:
Organic Process Research & Development. 27:322-330
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68bce8b5fad63c1cd64fa2a2bd5e1e90
https://doi.org/10.1021/acs.oprd.2c00348
https://doi.org/10.1021/acs.oprd.2c00348
Autor:
Lucas Bacheley, Ricardo Molina Betancourt, Rathies Ravindra, Gérard Guillamot, Phannarath Phansavath, Virginie Vidal
Publikováno v:
European Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bddb65cc5bef84390204a48a28d5cc9c
https://doi.org/10.1002/ejoc.202300383
https://doi.org/10.1002/ejoc.202300383
Autor:
Ricardo Molina Betancourt, Lucas Bacheley, Anzhela Karapetyan, Gérard Guillamot, Phannarath Phansavath, Virginie Ratovelomanana‐Vidal
Publikováno v:
ChemCatChem. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f3a4a7b618e29dbdb3faa3d6e2d0e7a
https://doi.org/10.1002/cctc.202200595
https://doi.org/10.1002/cctc.202200595
Autor:
Anne Westermeyer, Phannarath Phansavath, Virginie Ratovelomanana-Vidal, Quentin Llopis, Gérard Guillamot
Publikováno v:
Synlett. 31:1172-1176
A regioselective synthesis of 3,5-disubstituted pyrazoles was achieved by 1,3-dipolar cycloaddition of diazo compounds, generated in situ from N-tosylhydrazones, with unactivated bromovinyl acetals, which served as alkyne surrogates. The reaction tol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4cec79f34a65168b30ea03b1f1d1bd9
https://doi.org/10.1055/s-0039-1690885
https://doi.org/10.1055/s-0039-1690885
Publikováno v:
New Journal of Chemistry. 44:20535-20543
The access to a new family of unusual 4-fluorinated pyrazoles bearing acetal moities at the 3- or 5-position has been achieved by electrophilic fluorination using Selectfluor® with yields up to 67%. The unconverted starting material can be recovered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f2b2cabd35464bddf04dc022bec07c7
https://doi.org/10.1039/d0nj05222a
https://doi.org/10.1039/d0nj05222a
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2020, 76, pp.131221-. ⟨10.1016/j.tet.2020.131221⟩
Tetrahedron, Elsevier, 2020, 76, pp.131221-. ⟨10.1016/j.tet.2020.131221⟩
The copper-catalyzed cycloisomerization of alkynylaziridines has been developed to access 2-substituted-4-formylpyrroles. The reaction proved to be tolerant to aryl and alkyl-substituted substrates which were readily prepared from the corresponding e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69a2762aa7a16921124707722f09bea7
https://hal.archives-ouvertes.fr/hal-03493777
https://hal.archives-ouvertes.fr/hal-03493777
Publikováno v:
Organic letters. 22(10)
The asymmetric reduction of β-keto-γ-acetal enamides has been investigated. A wide range of enantioenriched β-hydroxy-γ-acetal enamides were obtained through asymmetric transfer hydrogenation catalyzed by a tethered Rh(III)-DPEN complex with yiel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e68d3c5eed09c5f7c92e2750ae9fb2e0
https://pubmed.ncbi.nlm.nih.gov/32330052
https://pubmed.ncbi.nlm.nih.gov/32330052
Autor:
Janine Cossy, Gérard Guillamot, Alexandre Dupas, Christophe Meyer, Pierre-Alexandre Lhotellier
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2019, 21 (10), pp.3589-3593. ⟨10.1021/acs.orglett.9b00999⟩
Organic Letters, American Chemical Society, 2019, 21 (10), pp.3589-3593. ⟨10.1021/acs.orglett.9b00999⟩
Bicyclic aziridines possessing a 1-azabicyclo[4.1.0]heptan-2-one core were prepared from 2 H-azirines by a stepwise annulation sequence involving a diastereoselective allylindanation, an N-acylation, and a ring-closing metathesis to construct the six
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4ad562e62839898e03b28cc038faf1a
https://hal.archives-ouvertes.fr/hal-02379813
https://hal.archives-ouvertes.fr/hal-02379813
Autor:
Gérard Guillamot, Quentin Llopis, Charlène Férard, Virginie Ratovelomanana-Vidal, Phannarath Phansavath
Publikováno v:
Synthesis. 48:3357-3363
A mild catalytic asymmetric transfer hydrogenation of a series of α-amino β-keto ester hydrochlorides catalyzed by a rhodium(III) complex is reported. The use of the formic acid/triethylamine system as the hydrogen donor source provided the corresp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64e97d90c50666c6b198750579cfddbb
https://doi.org/10.1055/s-0035-1562444
https://doi.org/10.1055/s-0035-1562444