Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kenji P. M. Kopf"'
Autor:
Luis F. Valdez Pérez, Sylvestre P. J. T. Bachollet, Nikolai V. Orlov, Kenji P. M. Kopf, Joseph P. A. Harrity
Publikováno v:
Angewandte Chemie International Edition. 62
We report that axially chiral biaryl boronic esters can be generated with control of atroposelectivity by a Binol-mediated dynamic thermodynamic resolution process. These intermediates can be progressed to enantioenriched products through stereoreten
Autor:
Mathias S. Hvid, Nina Lock, Amparo Sanz-Marco, Kenji P. M. Kopf, Sergio Carrasco, Belén Martín-Matute, Pedro J. Tortajada, Aitor Bermejo-López
Publikováno v:
Bermejo-López, A, Carrasco, S, Tortajada, P J, Kopf, K P M, Sanz-Marco, A, Hvid, M S, Lock, N & Martín-Matute, B 2021, ' Selective Synthesis of Imines by Photo-Oxidative Amine Cross-Condensation Catalyzed by PCN-222(Pd) ', ACS Sustainable Chemistry and Engineering, vol. 9, no. 43, pp. 14405-14415 . https://doi.org/10.1021/acssuschemeng.1c04389
Palladium-metalated PCN-222 enables the aerobic photo-oxidative cross-condensation of anilines with benzylic amines yielding a series of linear and cyclic imines. The reaction is very efficient under mild conditions, which allows the isolation of sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0a77bd34f6d69527151c683cf53fc19
https://pure.au.dk/portal/da/publications/selective-synthesis-of-imines-by-photooxidative-amine-crosscondensation-catalyzed-by-pcn222pd(614836e0-c0e2-4f9f-a03c-5a86a3c0f7c6).html
https://pure.au.dk/portal/da/publications/selective-synthesis-of-imines-by-photooxidative-amine-crosscondensation-catalyzed-by-pcn222pd(614836e0-c0e2-4f9f-a03c-5a86a3c0f7c6).html
Autor:
Joseph P. A. Harrity, Elliot J. McColl, Yee Hwee Lim, David L. Cousins, Werngard Czechtizky, Prisca Fricero, Kenji P. M. Kopf
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie (International Ed. in English)
Angewandte Chemie (International Ed. in English)
We report a novel and general method to access a highly under‐studied privileged scaffold—pyrimidines bearing a trifluoroborate at C4, and highlight the broad utility of these intermediates in a rich array of downstream functionalization reaction