Zobrazeno 1 - 10
of 153
pro vyhledávání: '"S. J. Proctor"'
Publikováno v:
CHIMIA, Vol 77, Iss 7/8 (2023)
Externí odkaz:
https://doaj.org/article/f1a86ec7ed6642fda0e44a3ba89a38e4
Autor:
Bao-Sheng Li, Yuhuang Wang, Rupert S. J. Proctor, Yuexia Zhang, Richard D. Webster, Song Yang, Baoan Song, Yonggui Robin Chi
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-8 (2016)
Benzyl bromides can be activated for radical reactions by photocatalytic single electron transfer. Here the authors show thatN-heterocyclic carbenes are also capable of activating this pathway for nitrobenzyl bromides, and that the radical intermedia
Externí odkaz:
https://doaj.org/article/f5b0f77486ea464ea415a0200b949e73
Publikováno v:
Journal of the American Chemical Society
Minisci-type reactions constitute one of the most powerful methods for building up complexity around basic heteroarenes. The most desirable variants involve formal oxidative coupling of a C-H bond on each partner, leading back to the simplest possibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02c43a24d8644c50a95beb9cf0b00e1d
https://doi.org/10.1021/jacs.1c01556
https://doi.org/10.1021/jacs.1c01556
Autor:
Robert J. Phipps, Rupert S. J. Proctor
Publikováno v:
Angewandte Chemie. 131:13802-13837
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d4486e1fd1526ab3785712079624f28
https://doi.org/10.1002/ange.201900977
https://doi.org/10.1002/ange.201900977
Publikováno v:
Nature Chemistry
The past decade has seen unprecedented growth in the development of new chemical methods that proceed by mechanisms involving radical intermediates. This new attention has served to highlight a long-standing challenge in the field of radical chemistr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64c588c89f91e35bcd9f1ea41ec2a657
https://pubmed.ncbi.nlm.nih.gov/33208895
https://pubmed.ncbi.nlm.nih.gov/33208895
Publikováno v:
Journal of the American Chemical Society
The Minisci reaction is one of the most direct and versatile methods for forging new carbon-carbon bonds onto basic heteroarenes: a broad subset of compounds ubiquitous in medicinal chemistry. While many Minisci-type reactions result in new stereocen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::716af8a5a9208dd9e701ed20bb3e8e64
Publikováno v:
Nature Chemistry. 13:99-99
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c826a81c763c299ab58f001abcf22de
https://doi.org/10.1038/s41557-020-00590-1
https://doi.org/10.1038/s41557-020-00590-1
Publikováno v:
Science (New York, N.Y.). 360(6387)
Basic heteroarenes are a ubiquitous feature of pharmaceuticals and bioactive molecules, and Minisci-type additions of radical nucleophiles are a leading method for their elaboration. Despite many Minisci-type protocols that result in the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ffa135a1d4d1d801a596c4fc0dddbbd4
https://pubmed.ncbi.nlm.nih.gov/29622723
https://pubmed.ncbi.nlm.nih.gov/29622723
Publikováno v:
ChemInform. 47
The introduction of a chlorine atom to a carbon center in an enantioselective manner via conventional C–Cl bond formation is difficult. Here we report a new approach to this class of tertiary alkyl chlorides with high optical purities. Instead of f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::568e82eea053d996e0d1497d180edb15
https://doi.org/10.1002/chin.201643085
https://doi.org/10.1002/chin.201643085
Publikováno v:
Chemical communications (Cambridge, England). 52(53)
The introduction of a chlorine atom to a carbon center in an enantioselective manner via conventional C–Cl bond formation is difficult. Here we report a new approach to this class of tertiary alkyl chlorides with high optical purities. Instead of f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb88a279896edcd0b19209a8fe002148
https://pubmed.ncbi.nlm.nih.gov/27298081
https://pubmed.ncbi.nlm.nih.gov/27298081