Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Andrew C. Hones"'
Publikováno v:
European Journal of Organic Chemistry, 2022, Vol.2022(47) [Peer Reviewed Journal]
The iridium catalysed C−H borylation of polyfluorinated arenes and heteroarenes occurs rapidly and efficiently. As with other borylation reactions, whilst steric parameters dominate, an underlying electronic influence on reaction selectivity can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1afb28e69ca3319cdc893c7f97414d14
https://doi.org/10.1002/ejoc.202201005
https://doi.org/10.1002/ejoc.202201005
Autor:
Andrew C. Hones, Scott A. Sadler, Todd B. Marder, Patrick G. Steel, David C. Blakemore, Bryan Roberts
Publikováno v:
ChemInform. 46
In the absence of any steric directing group, the title reaction proceeds selectively at C-3 of the indazole skeleton.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c190a8c5c1d7c1541ac531717f5ab10
https://doi.org/10.1002/chin.201540148
https://doi.org/10.1002/chin.201540148
Autor:
Bryan Roberts, Scott A. Sadler, Todd B. Marder, Patrick G. Steel, Andrew C. Hones, David C. Blakemore
Publikováno v:
Journal of organic chemistry, 2015, Vol.80(10), pp.5308-5314 [Peer Reviewed Journal]
In the absence of a steric directing group, iridium-catalyzed C–H borylation of N-protected indazoles occurs rapidly and selectively at C-3 and the resulting boronate esters can be utilized in a range of downstream conversions. The functional group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f7972347a23b3dda9fe11905c62d09
https://pubmed.ncbi.nlm.nih.gov/25894824
https://pubmed.ncbi.nlm.nih.gov/25894824