Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yasuyo Tahara"'
Autor:
Masakazu Nambo, Jacky C.-H. Yim, Luiza B. O. Freitas, Yasuyo Tahara, Zachary T. Ariki, Yuuki Maekawa, Daisuke Yokogawa, Cathleen M. Crudden
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-7 (2019)
α-Fluoromethyl arenes are common substructures in pharmaceuticals and agrochemicals but synthetic routes are still rare. Here the authors describe Pd-catalyzed Suzuki-Miyaura cross-coupling of α-fluorinated benzylic triflones with arylboronic acids
Externí odkaz:
https://doaj.org/article/85482d2823a043c0b578abf6eb4fb873
Autor:
Masakazu Nambo, Koushik Ghosh, Jacky C.-H. Yim, Yasuyo Tahara, Naoto Inai, Takeshi Yanai, Cathleen M. Crudden
Publikováno v:
ACS Catalysis. 12:9526-9532
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e696afd5f3bbabd7f18b86d0f05f3b0
https://doi.org/10.1021/acscatal.2c02233
https://doi.org/10.1021/acscatal.2c02233
Publikováno v:
Canadian Journal of Chemistry.
The synthesis of gem-difluoroalkenes by photocatalytic desulfonylative coupling of alkylsulfones with α-(trifluoromethyl)styrenes is described. Photoredox Ir complex was found to be an effective catalyst for this transformation through single electr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d0afd734a1fc099f450adfacfb61f75
https://doi.org/10.1139/cjc-2022-0271
https://doi.org/10.1139/cjc-2022-0271
Publikováno v:
Chemical Science
A new method for the generation of tertiary radicals through single electron reduction of alkylsulfones promoted by Zn and 1,10-phenanthroline has been developed. These radicals could be employed in the Giese reaction, affording structurally diverse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1076e927d0189092309eef42bfe22e28
https://doi.org/10.1039/d1sc00133g
https://doi.org/10.1039/d1sc00133g
Publikováno v:
Chemistry Letters. 48:975-977
The synthesis of azole-containing triarylmethanes via the Cu-catalyzed desulfonylative reaction of benzhydryl sulfone derivatives with azoles is described. Various azoles such as 1,3-thiazole and 1...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e356464122fe198842f87f27dcab108f
https://doi.org/10.1246/cl.190334
https://doi.org/10.1246/cl.190334
Autor:
Daisuke Yokogawa, Masakazu Nambo, Cathleen M. Crudden, Yuuki Maekawa, Jacky C.-H. Yim, Zachary T. Ariki, Luiza B. O. Freitas, Yasuyo Tahara
Publikováno v:
Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-7 (2019)
Nature Communications, Vol 10, Iss 1, Pp 1-7 (2019)
α-Fluoromethylarenes are common substructures in pharmaceuticals and agrochemicals, with the introduction of fluorine often resulting in improved biological activity and stability. Despite recent progress, synthetic routes to α-fluorinated diarylme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b66e421c34132b592b0a79152113057
https://doi.org/10.1038/s41467-019-11758-w
https://doi.org/10.1038/s41467-019-11758-w
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(8)
A new method for the synthesis of benzhydryl amines from the reaction of readily available sulfone derivatives with amines is described. The Cu-catalyzed desulfonylative amination not only provides structurally diverse benzhydryl amines in good yield
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6206f13bf70e1160f07e0073d01ec1ef
https://pubmed.ncbi.nlm.nih.gov/30450672
https://pubmed.ncbi.nlm.nih.gov/30450672