Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nicholas J. Race"'
Publikováno v:
Org Lett
We report that the treatment of unsymmetrical 2,3-disubstituted aziridines with TiCl(4) yields β-phenethylamine products via the intermediacy of a phenonium ion. Derivatization of the products obtained via this method is demonstrated. Computational
Publikováno v:
The Journal of organic chemistry.
We report the dual-catalytic enantioselective allylic alkylation of 2-(pyridylmethyl)amine-derived ketimines with allylic carbonates. The reaction proceeds under mild reaction conditions to generate α-amino heteroaryl benzylamine stereocenters in go
Publikováno v:
The Journal of Organic Chemistry.
Publikováno v:
Synlett. 32:01-06
Formation of phenonium ions through anchimeric assistance (neighboring-group participation) of aryl rings has been known since 1949. Although these reactive intermediates have been studied extensively by physical organic chemists, their potential as
Publikováno v:
Journal of the American Chemical Society. 142:8090-8096
We report the first examples of selective and regiodivergent opening of unsymmetrical phenonium ions with chloride ions. These reactions are enabled by the dual role of SnCl4 and TiCl4 as Lewis acids and chloride nucleophiles. Reagent control dictate
Publikováno v:
Chemical Science
Race, N J, Hazelden, I R, Faulkner, A & Bower, J F 2017, ' Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles ', Chemical Science, vol. 8, no. 8, pp. 5248-5260 . https://doi.org/10.1039/c7sc01480e
Race, N J, Hazelden, I R, Faulkner, A & Bower, J F 2017, ' Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles ', Chemical Science, vol. 8, no. 8, pp. 5248-5260 . https://doi.org/10.1039/c7sc01480e
The scope and mechanism of aza-Heck methodologies that provide chiral heterocyclic systems are outlined.
Aza-Heck cyclizations are an emerging method for the construction of chiral N-heterocyclic systems. In these processes, an activated N–O b
Aza-Heck cyclizations are an emerging method for the construction of chiral N-heterocyclic systems. In these processes, an activated N–O b
Publikováno v:
Journal of the American Chemical Society. 138:15881-15884
An enantioselective intermolecular coupling of oxygen nucleophiles and allylic alcohols to give β-aryloxycarbonyl compounds is disclosed using a chiral pyridine oxazoline-ligated palladium catalyst under mild conditions. As opposed to the formation
Publikováno v:
Race, N J, Faulkner, A, Shaw, M H & Bower, J 2016, ' Dichotomous mechanistic behaviour in Narasaka-Heck cyclizations: electron rich Pd-catalysts generate iminyl radicals ', Chemical Science, vol. 7, no. 2, pp. 1508-1513 . https://doi.org/10.1039/C5SC04037J
Chemical Science
Chemical Science
Pd-catalyzed cyclizations of oxime esters with pendant alkenes undergo ligand controlled mechanistic divergence. Electron deficient phosphines promote aza-Heck cyclization; electron rich systems favour a SET pathway. Mechanistic experiments different
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(2)
A palladium-catalyzed enantioselective redox-relay Heck reaction of 2-indole triflates and disubstituted alkenes is reported. This process combines readily available indole triflates with a variety of alkenes to afford a range of indole derivatives b
Autor:
N. Rodríguez, J.-P. Lumb, T. M. Leuther, A. C. Wright, Anna Andries-Ulmer, Takao Ikariya, C. Gimbert-Suriñach, Kazuaki Ishihara, P. Calleja, R. Dorel, Z. Li, B. M. Stoltz, G. Liu, F. Bellina, L. A. Perego, L. M. Dornan, P. J. Pérez, Fateh V. Singh, N. L. Hughes, Matthew S. Sigman, N. Jiao, M. J. Muldoon, Muhammet Uyanik, M. Borrell, Kilian Muñiz, R. Gómez-Arrayas, Pau Farràs, D. C. Ebner, T. Wdowik, M. M. Díaz-Requejo, Antoni Llobet, A. Caballero, Nicholas J. Race, Hauke Engler, Yoshihito Kayaki, S. R. Chemler, Thomas Wirth, I. Funes-Ardoiz, P. Chen, Pablo Garrido-Barros, Harshkumar H. Patel, K. V. N. Esguerra, Tanja Gulder, N. Park, L. Vicens, Miquel Costas, A. M. Echavarren, S. Sillner, Claudio Martínez, Albrecht Berkessel, A. G. Griesbeck, M. Kleczka, F. Maseras
Publikováno v:
Science of Synthesis ISBN: 9783132403710
Catalytic Oxidation in Organic Synthesis
Catalytic Oxidation in Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41e4590745a984aa3d12cc2147b0527f
https://doi.org/10.1055/b-003-129345
https://doi.org/10.1055/b-003-129345