Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Brendan J. Fallon"'
Publikováno v:
ChemistrySelect. 5:15190-15194
Autor:
Richard P. Marshall, John Martin Pritchard, Josie Morrell, Simon J. F. Macdonald, Seble Lemma, John F. Barrett, Paula Saklatvala, Robert J. Slack, Panayiotis A. Procopiou, Joelle Le, Tim N. Barrett, Ashley Paul Hancock, James E. Rowedder, Matthew H. J. Crawford, Anderson Niall Andrew, Giovanni Vitulli, Colin J. Suckling, Brendan J. Fallon, Steven L. Sollis, Lee R. Thorp
Publikováno v:
Journal of Medicinal Chemistry. 61:8417-8443
A series of 3-aryl(pyrrolidin-1-yl)butanoic acids were synthesized using a diastereoselective route, via a rhodium catalyzed asymmetric 1,4-addition of arylboronic acids in the presence of (R)-BINAP to a crotonate ester to provide the (S) absolute co
Autor:
Sean M. Lynn, Brendan J. Fallon, Simon J. F. Macdonald, Ian B. Campbell, Steven L. Sollis, Panayiotis A. Procopiou, Lee R. Thorp, Anderson Niall Andrew, John Martin Pritchard
Publikováno v:
Organic & Biomolecular Chemistry. 14:5992-6009
A diastereoselective synthesis of (S)-3-(3-(3,5-dimethyl-1H-pyrazol-1-yl)phenyl)-4-((R)-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)butanoic acid (1), a potential therapeutic agent for the treatment of Idiopathic Pulmonary Fi
Autor:
Panayiotis A, Procopiou, Niall A, Anderson, John, Barrett, Tim N, Barrett, Matthew H J, Crawford, Brendan J, Fallon, Ashley P, Hancock, Joelle, Le, Seble, Lemma, Richard P, Marshall, Josie, Morrell, John M, Pritchard, James E, Rowedder, Paula, Saklatvala, Robert J, Slack, Steven L, Sollis, Colin J, Suckling, Lee R, Thorp, Giovanni, Vitulli, Simon J F, Macdonald
Publikováno v:
Journal of medicinal chemistry. 61(18)
A series of 3-aryl(pyrrolidin-1-yl)butanoic acids were synthesized using a diastereoselective route, via a rhodium catalyzed asymmetric 1,4-addition of arylboronic acids in the presence of ( R)-BINAP to a crotonate ester to provide the ( S) absolute
Autor:
Ye Lyu, Muriel Amatore, Laura Ferrand, Marc Petit, Alejandro Rivera-Hernández, Corinne Aubert, Brendan J. Fallon
Publikováno v:
Synthesis
Synthesis, 2017, 49 (17), pp.3895--3904. ⟨10.1055/s-0036-1588996⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2017, 49 (17), pp.3895--3904. ⟨10.1055/s-0036-1588996⟩
Synthesis, 2017, 49 (17), pp.3895--3904. ⟨10.1055/s-0036-1588996⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2017, 49 (17), pp.3895--3904. ⟨10.1055/s-0036-1588996⟩
The use of a simple well-defined low-valent cobalt(I) catalyst [HCo(PMe3)4] capable of performing the regio- and stereoselective hydroboration of internal alkynes is reported. Extension to the diboration of internal alkynes is also related using the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10686b354e7436ef29943cc4dcb50a2d
https://hal.archives-ouvertes.fr/hal-01644384
https://hal.archives-ouvertes.fr/hal-01644384
Autor:
Cédric Simon, Geoffrey Gontard, Muriel Amatore, Etienne Derat, Marc Petit, Alejandro Rivera-Hernández, Sandrine Ventre, Marie-Hélène Tremblay, Corinne Aubert, Brendan J. Fallon
Publikováno v:
Organic Letters
Organic Letters, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩
Organic Letters, American Chemical Society, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩
Organic Letters, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩
Organic Letters, American Chemical Society, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩
International audience; Herein, the use of a well-defined low-valent cobalt(I) catalyst [HCo(PMe3)(4)] capable of performing the highly regio- and stereoselective hydrosilylation of internal alkynes is reported. The reaction can be applied to a varie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63efcd214bf60852cd64acc101c7bb54
https://hal.science/hal-01397954
https://hal.science/hal-01397954
Autor:
Brendan J. Fallon, Muriel Amatore, Corinne Aubert, Marc Petit, Franck Ferreira, Alejandro Perez-Luna, Fabrice Chemla, Etienne Derat
Publikováno v:
ChemInform. 47
Herein an extremely versatile, well-defined, low-valent cobalt catalyst [Co(PMe3)4] capable of intermolecular and intramolecular imine-directed C2-alkylation and alkenylation of indoles is reported. The reaction proceeds in the absence of reducing ag
Autor:
Corinne Aubert, Etienne Derat, Muriel Amatore, Marc Petit, Alejandro Perez-Luna, Brendan J. Fallon, Franck Ferreira, Fabrice Chemla
Publikováno v:
Organic Letters
Organic Letters, 2016, 18 (9), pp.2292-2295. ⟨10.1021/acs.orglett.6b00939⟩
Organic Letters, American Chemical Society, 2016, 18 (9), pp.2292-2295. ⟨10.1021/acs.orglett.6b00939⟩
Organic Letters, 2016, 18 (9), pp.2292-2295. ⟨10.1021/acs.orglett.6b00939⟩
Organic Letters, American Chemical Society, 2016, 18 (9), pp.2292-2295. ⟨10.1021/acs.orglett.6b00939⟩
International audience; Herein an extremely versatile, well-defined, low-valent cobalt catalyst [Co(PMe3)(4)] capable of intermolecular and intramolecular imine-directed C2-alkylation and alkenylation of indoles is reported. The reaction proceeds in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dea33d5bbcc4cbde6bb46d9ae95354a
https://hal.science/hal-01397956
https://hal.science/hal-01397956
Autor:
Vincent Corcé, Franck Ferreira, Muriel Amatore, Alejandro Perez-Luna, Marc Petit, Fabrice Chemla, Corinne Aubert, Brendan J. Fallon
Publikováno v:
New J. Chem.
New J. Chem., 2016, 40 (12), pp.9912--9916. ⟨10.1039/C6NJ03265F⟩
New J. Chem., 2016, 40 (12), pp.9912--9916. ⟨10.1039/C6NJ03265F⟩
International audience; Herein, we report the first catalytic version of a cobalt-catalysed reductive homocoupling of benzyl halides which proceeds with low catalyst loadings (0.5 to 5 mol%). By synthetizing each cobalt intermediate we demonstrate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b33b7e1ba417f8531713d3a0061cb35
https://hal.archives-ouvertes.fr/hal-01638307
https://hal.archives-ouvertes.fr/hal-01638307
Autor:
Elena Valverde, John Martin Pritchard, Allan J. B. Watson, Colin J. Suckling, Anderson Niall Andrew, Brendan J. Fallon, Simon J. F. Macdonald
Publikováno v:
Synlett. 23:2817-2821
Application of the Miyaura–Hayashi rhodium-catalysed addition of aryl boronic acids to acyclic unsaturated esters featuring basic centres to yield γ-amino butyric acids incorporating a substituted β-phenyl group is described. Unoptimised isolated