Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mark W. Campbell"'
Autor:
Scott T. Shreiber, Albert Granados, Bianca Matsuo, Jadab Majhi, Mark W. Campbell, Shivani Patel, Gary A. Molander
Publikováno v:
Organic Letters. 24:8542-8546
An aryl disulfide mediated C-F bond activation of the trifluoromethyl group to generate valuable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bc5a4d203e1ee66fc94c91c826f35d1
https://doi.org/10.1021/acs.orglett.2c03549
https://doi.org/10.1021/acs.orglett.2c03549
Publikováno v:
J Am Chem Soc
An intermolecular, photocatalytic dicarbofunctionalization (DCF) of olefins enabled by the merger of Giese-type addition with Ni/photoredox dual catalysis has been realized. Capitalizing on the rapid addition of 3° radicals to alkenes and their relu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2169ef0f772a7c28354f44189bba787
https://doi.org/10.1021/jacs.9b08282
https://doi.org/10.1021/jacs.9b08282
Autor:
Jadab Majhi, Gary A. Molander, Viktor C. Polites, Shivani A. Patel, Mark W. Campbell, Juliette E. Lipson
Publikováno v:
J Am Chem Soc
The installation of gem-difluoromethylene groups into organic structures remains a daunting synthetic challenge despite their attractive structural, physical, and biochemical properties. A very efficient retrosynthetic approach would be the functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::624d6fcc69af9642a57f7511af5eb467
https://pubmed.ncbi.nlm.nih.gov/34793157
https://pubmed.ncbi.nlm.nih.gov/34793157
Publikováno v:
J Am Chem Soc
Alkenes, ethers, and alcohols account for a significant percentage of bulk reagents available to the chemistry community. The petrochemical, pharmaceutical, and agrochemical industries each consume gigagrams of these materials as fuels and solvents e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c64d5d4b2586fa1653ba8ec1297caa1
https://pubmed.ncbi.nlm.nih.gov/33660996
https://pubmed.ncbi.nlm.nih.gov/33660996
A mild, metal-free, regioselective carbofluorination of dehydroalanine derivatives has been developed. Alkyl radicals resulting from visible-light photoredox catalysis engage in a radical conjugate addition to dehydroalanine, with subsequent fluorina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::824e10d0ec6b977dd44bfb0932dc4320
https://europepmc.org/articles/PMC6777868/
https://europepmc.org/articles/PMC6777868/
