Zobrazeno 1 - 10
of 227
pro vyhledávání: '"Jack R, Norton"'
Publikováno v:
JACS Au, Vol 3, Iss 12, Pp 3366-3373 (2023)
Externí odkaz:
https://doaj.org/article/ddd0fc28241a411ba742084055fde7e3
Publikováno v:
ACS Sustainable Chemistry & Engineering. 10:11106-11116
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20c9e5ba3ed63b22dc086d3694469622
https://doi.org/10.1021/acssuschemeng.2c01404
https://doi.org/10.1021/acssuschemeng.2c01404
Publikováno v:
Nature Synthesis. 1:313-321
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f0abe63e9652367017ce15deaa05e03
https://doi.org/10.1038/s44160-022-00051-2
https://doi.org/10.1038/s44160-022-00051-2
Publikováno v:
J Am Chem Soc
Under mild conditions (room temperature, 80 psi of H(2)) Cp*Rh(2-(2-pyridyl)phenyl)H catalyzes the selective hydrogenation of the C═C bond in α,β-unsaturated carbonyl compounds, including natural product precursors with bulky substituents in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fdd4905ad4b62d44a5f8cd1f0babf92
https://doi.org/10.1021/jacs.1c04683
https://doi.org/10.1021/jacs.1c04683
Autor:
Jack R. Norton, Hagen Neugebauer, Andreas Hansen, Markus Bursch, Hunter B. Vibbert, Stefan Grimme
Publikováno v:
Canadian Journal of Chemistry. 99:216-220
The H• transfer rate constants for a series of group 6 molybdenum and tungsten pyrazolyl borate complexes are described. The rate constants for these complexes were found to span a range over 1 magnitude. Analysis of the H• transfer rate constant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98f9c947e56135ed669eed0514ed1005
https://doi.org/10.1139/cjc-2020-0392
https://doi.org/10.1139/cjc-2020-0392
Autor:
Alexander P. Aydt, Chengbo Yao, Jiawei Chen, Steffen Jockusch, Michael Rauch, Jack R. Norton, Amymarie K. Bartholomew, Hunter B. Vibbert, Matthew Hammond
Publikováno v:
Organometallics. 39:4592-4598
We report herein the reactions of the Rosenthal complexes, Cp2Ti(BTMSA) and Cp*2Ti(BTMSA) (BTMSA: bis(trimethylsilyl)acetylene), with CpCr(CO)3H. Those complexes are known to dissociate their alkyn...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f60c8d1bda79fe5bbc7ad4a2e6e4ca3
https://doi.org/10.1021/acs.organomet.0c00645
https://doi.org/10.1021/acs.organomet.0c00645
Publikováno v:
Org Lett
We have found that terminal N-vinylindoles bearing cycloalkanone substituents are excellent hydrogen atom acceptors, generating α-aminyl radicals with a variety of catalysts (Co(II)/H(2) or Co(III)Cl precatalysts with silane reductants). These radic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffc0149f7388cd6fa288784b1640459a
https://doi.org/10.1021/acs.orglett.0c02272
https://doi.org/10.1021/acs.orglett.0c02272
Publikováno v:
The Journal of organic chemistry. 87(7)
A Ti/Cr cooperative catalyst isomerizes aziridines to allyl amines under mild conditions. The reaction tolerates a broad range of aziridines with various nitrogen substituents. The titanium catalyst is most successful in opening 1,2-disubstituted azi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce8a840cc2a5b64b5b310e809ba484a7
https://pubmed.ncbi.nlm.nih.gov/35303410
https://pubmed.ncbi.nlm.nih.gov/35303410
Autor:
Scott A. Snyder, Farbod Salahi, Shicheng Shi, Jack R. Norton, Maleeha Rahman, Hunter B. Vibbert
Publikováno v:
Angew Chem Int Ed Engl
Carbon-centered radicals can be stabilized by delocalization of their spin density into the vacant p orbital of a boron substituent. α-Vinyl boronates, in particular pinacol (Bpin) derivatives, are excellent hydrogen atom acceptors. Under H(2), in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eda4a8fc9032a720dd08c5f1321ea6a
https://europepmc.org/articles/PMC8582025/
https://europepmc.org/articles/PMC8582025/
Over millennia, Nature has evolved exquisite synthetic pathways that combine isoprenes into chains, folds them into carbocycles, and then oxidizes/rearranges them into vast complexity (>50,000 members). While laboratory chemical synthesis can sometim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0386f0cc841b2c692aabce728d51a558
https://doi.org/10.33774/chemrxiv-2021-m5q24
https://doi.org/10.33774/chemrxiv-2021-m5q24