Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bryan C Figula"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-11 (2024)
Abstract Fluorinated organic compounds are frequently used across the chemical and life sciences. Although a large, structurally diverse pool of alkyl fluorides is nowadays available, synthetic applications trail behind the widely accepted utility of
Externí odkaz:
https://doaj.org/article/69e7a690d9e84ad3be6fda1bb460bf97
Publikováno v:
Organic Letters. 24:8719-8723
Cross-coupling of alkyl fluorides and organocuprates is accomplished via aluminum halide mediated C-F bond activation and subsequent C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58b9e65c49a8a46e859d64f64e9f2a4d
https://doi.org/10.1021/acs.orglett.2c03775
https://doi.org/10.1021/acs.orglett.2c03775
Publikováno v:
ACS Catalysis. 12:11854-11859
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f25714a238f75b2603efde79730281f
https://doi.org/10.1021/acscatal.2c02474
https://doi.org/10.1021/acscatal.2c02474
Autor:
Bryan C. Figula, Stefan Wiese, Jeffery A. Bertke, Christine Greene, Abolghasem Bakhoda, Timothy H. Warren
Publikováno v:
Organometallics. 39:1710-1718
The dinuclear β-diketiminato NiII tert-butoxide {[Me3NN]Ni}2(μ-OtBu)2 (2), synthesized from [Me3NN]Ni(2,4-lutidine) (1) and di-tert-butylperoxide, is a versatile precursor for the synthesis of a se...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42185b0f0dfb38a892bb73cb27db7dc1
https://doi.org/10.1021/acs.organomet.0c00021
https://doi.org/10.1021/acs.organomet.0c00021
Autor:
Timothy H. Warren, Jeffery A. Bertke, Bryan C. Figula, Christine Greene, Stefan Wiese, Abolghasem (Gus) Bakhoda
The dinuclear b-diketiminato NiIItert-butoxide {[Me3NN]Ni}2(μ-OtBu)2 (2), synthesized from [Me3NN]Ni(2,4-lutidine) (1) and di-tert-butylperoxide, is a versatile precursor for the synthesis of a series of NiIIcomplexes [Me3NN]Ni-FG to illustrate C-C,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::964249a6c55ce84ffc0a05c1e7a375be
https://doi.org/10.26434/chemrxiv.8115860.v1
https://doi.org/10.26434/chemrxiv.8115860.v1
Autor:
Sarah J Burke, John W. Tomsho, James M. Gamrat, Nicholas R Sadowski, Bryan C Figula, Giulia Mancini, Rebecca C Colandrea
Publikováno v:
The Journal of organic chemistry. 83(11)
The synthesis and utility of three benzoxaborole protecting groups are reported. These protecting groups improve organic solubility and allow otherwise incompatible reactions (oxidations, substitutions, and mild reductions) to be achieved in the pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b5a2648a79675aefc7e60e8ef239dff
https://pubmed.ncbi.nlm.nih.gov/29724096
https://pubmed.ncbi.nlm.nih.gov/29724096