Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Marc Magre"'
Publikováno v:
Chemical reviews : CR 122(9), 8261-8312 (2022). doi:10.1021/acs.chemrev.1c00641
Chemical reviews : CR 122(9), 8261-8312 (2022). doi:10.1021/acs.chemrev.1c00641
Published by American Chemical Society Publ., Washington, DC
Published by American Chemical Society Publ., Washington, DC
Autor:
Josep Cornella, Marc Magre
Publikováno v:
Journal of the American Chemical Society
A Bi-catalyzed synthesis of sulfonyl fluorides from the corresponding (hetero)aryl boronic acids is presented. We demonstrate that the organobismuth(III) catalysts bearing a bis-aryl sulfone ligand backbone revolve through different canonical organom
Publikováno v:
Angewandte Chemie International Edition
(Hetero)arylsulfur compounds where the S atom is in the oxidation state VI represent a large percentage of the molecular functionalities present in organic chemistry. More specifically, (hetero)aryl-SVI fluorides have recently received enormous atten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09c60068a998d41e7ebead058e13e641
https://hdl.handle.net/21.11116/0000-000B-1BBD-321.11116/0000-000A-7133-D
https://hdl.handle.net/21.11116/0000-000B-1BBD-321.11116/0000-000A-7133-D
Autor:
Pol Cruz‐Sánchez, Maria Biosca, Marc Magre, Jorge Faiges, Jéssica Margalef, Oscar Pàmies, Montserrat Diéguez
Publikováno v:
European Journal of Inorganic Chemistry. 2022
Publikováno v:
Angewandte Chemie (International ed. in English). 61(23)
(Hetero)arylsulfur compounds where the S atom is in the oxidation state VI represent a large percentage of the molecular functionalities present in organic chemistry. More specifically, (hetero)aryl-S
Publikováno v:
Journal of the American Chemical Society 142(33), 14286-14294 (2020). doi:10.1021/jacs.0c05917
Journal of the American Chemical Society
Journal of the American Chemical Society
Journal of the American Chemical Society 142(33), 14286-14294 (2020). doi:10.1021/jacs.0c05917
Published by American Chemical Society, Washington, DC
Published by American Chemical Society, Washington, DC
Publikováno v:
Organic Letters. 22:3209-3214
A new reduction of carbamates to N-methyl amines is presented. The magnesium-catalyzed reduction reaction allows the conversion of cyclic and linear carbamates, including N-Boc protected amines, in...
Publikováno v:
Organic Letters. 22:1594-1598
A regio- and stereoselective magnesium-catalyzed hydrostannylation of internal and terminal alkynes has been developed. Excellent yields and selectivities are obtained for a wide range of terminal and internal symmetrical and unsymmetrical alkynes by
Publikováno v:
ACS Catalysis. 9:11634-11639
Efficient reduction of cyclic and linear organic carbonates catalyzed by a readily available earth alkaline catalyst has been achieved. The described homogenous reaction based on a ligand-free magnesium catalyst provides an indirect route for the con
Publikováno v:
Organic Letters. 21:9153-9157
A simple and efficient catalytic system for a chemo- and regioselective ortho-alkenylation of anilines is presented. The new magnesium-catalyzed reaction allows the use of a wide range of alkynes and anilines with different electronic and steric prop