Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Trevor V. Nykaza"'
Autor:
Trevor V. Nykaza, Julian C. Cooper, Alexander T. Radosevich, Robert‐Cristian Raclea, Kyan A. D'Angelo, Mohammad Movassaghi
Publikováno v:
Organic Syntheses. :1-18
Autor:
Alexander T. Radosevich, Julian C. Cooper, Michael R. Luzung, Antonio Ramirez, Gen Li, Trevor V. Nykaza
Publikováno v:
Journal of the American Chemical Society. 142:6786-6799
Experimental, spectroscopic, and computational studies are reported that provide an evidence-based mechanistic description of an intermolecular reductive C-N coupling of nitroarenes and arylboronic acids catalyzed by a redox-active main-group catalys
Publikováno v:
PMC
Angew Chem Int Ed Engl
Angew Chem Int Ed Engl
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim An organocatalytic method for the modular synthesis of diverse N-aryl and N-alkyl azaheterocycles (indoles, oxindoles, benzimidazoles, and quinoxalinediones) is reported. The method employs a small-r
Publikováno v:
PMC
A method for the preparation of aryl- and heteroarylamine products by triethylphosphine-mediated deoxygenative coupling of nitroarenes and boronic acids is reported. This method provides access to an array of functionalized (hetero)arylamine products
Publikováno v:
Organic Syntheses
Prof. Radosevich via Ye Li
Prof. Radosevich via Ye Li
Publikováno v:
Organic Synth
[Image: see text]
Autor:
Nolwenn Mahieu, Julian C. Cooper, Gen Li, Trevor V. Nykaza, Michael R. Luzung, Alexander T. Radosevich, Antonio Ramirez
Publikováno v:
Journal of the American Chemical Society. 140:15200-15205
A main group-catalyzed method for the synthesis of aryl- and heteroarylamines by intermolecular C–N coupling is reported. The method employs a small-ring organophosphorus-based catalyst (1,2,2,3,4,4-hexamethylphosphetane) and a terminal hydrosilane
Autor:
Trevor V. Nykaza, Alexander T. Radosevich, Michael R. Luzung, Tyler S. Harrison, Antonio Ramirez
Publikováno v:
Journal of the American Chemical Society. 140:3103-3113
A small-ring phosphacycloalkane (1,2,2,3,4,4-hexamethylphosphetane, 3) catalyzes intramolecular C–N bond forming heterocyclization of o-nitrobiaryl and –styrenyl derivatives in the presence of a hydrosilane terminal reductant. The method provides
Publikováno v:
Journal of the American Chemical Society. 139:6839-6842
A small ring phosphacycle (1,2,2,3,4,4-hexamethylphosphetane) is found to catalyze deoxygenative N-N bond-forming Cadogan heterocyclization of o-nitrobenzaldimines, o-nitroazobenzenes and related substrates in the presence of hydrosilane terminal red
Publikováno v:
Tetrahedron
A method for the preparation of aryl- and heteroarylamine products by triethylphosphine-mediated deoxygenative coupling of nitroarenes and boronic acids is reported. This method provides access to an array of functionalized (hetero)arylamine products