Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Christopher B. Kelly"'
Autor:
Marian C. Bryan, Charlotte Dalton, Alba Díaz-Rodríguez, Jaika Doerfler, Oliver D. Engl, Alejandro Gimenez Molina, Vanessa Harawa, Christopher B. Kelly, Wei Li, Rachel H. Munday, Jan Pawlas, Paul F. Richardson, William J. Smith, Alan Steven, Balaram S. Takale, Jack A. Terrett, Daniel S. Treitler, Mingshuo Zeng
Publikováno v:
Organic Process Research & Development. 27:563-570
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75cfa86fb3968343526278f23eeebbad
https://doi.org/10.1021/acs.oprd.3c00065
https://doi.org/10.1021/acs.oprd.3c00065
Publikováno v:
Handbook of CH-Functionalization. :1-23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac6d0dced24c0968aab84d680090bdf
https://doi.org/10.1002/9783527834242.chf0211
https://doi.org/10.1002/9783527834242.chf0211
A Practical Oxidation Experiment for Undergraduate Students: Bobbitt’s Salt as a 'Green' Alternative
Autor:
Kyle M. Lambert, Christopher B. Kelly, John A. Milligan, Leon J. Tilley, Robert P. Reynolds, Kellen P. McGuire, Luigi Anzalone, Kimberly E. Del Sesto, Sinead Walsh
Publikováno v:
Journal of Chemical Education. 99:3249-3258
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::293f04ecfd246203a92f509f10d95843
https://doi.org/10.1021/acs.jchemed.2c00236
https://doi.org/10.1021/acs.jchemed.2c00236
Publikováno v:
Chemical Science. 13:11721-11737
The unique chemistry of small, strained carbocyclic systems has long captivated organic chemists from a theoretical and fundamental standpoint. A resurgence of interest in strained carbocyclic species has been prompted by their potential as bioisoste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8595cc3bcfcbf6c5a673bba8b6e292a
https://doi.org/10.1039/d2sc03948f
https://doi.org/10.1039/d2sc03948f
Autor:
Christopher B. Kelly
Publikováno v:
Organic Syntheses. 99:342-362
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f0e0addb95210f150b23337821b9fc
https://doi.org/10.15227/orgsyn.099.0342
https://doi.org/10.15227/orgsyn.099.0342
Autor:
Balu D. Dherange, Mingbin Yuan, Christopher B. Kelly, Christopher A. Reiher, Cristina Grosanu, Kathleen J. Berger, Osvaldo Gutierrez, Mark D. Levin
Publikováno v:
Journal of the American Chemical Society.
Selective functional group interconversions in complex molecular settings underpin many of the challenges facing modern organic synthesis. Currently, a privileged subset of functional groups dominates this landscape, while others, despite their abund
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::287dcb6ea27eaa3c0ccc7dffca72e5b6
https://pubmed.ncbi.nlm.nih.gov/36548788
https://pubmed.ncbi.nlm.nih.gov/36548788
Autor:
Sylvain Guizzetti, James A. Schwindeman, David S. B. Daniels, James J. Douglas, Alex Kosanovich, James P. Phelan, Wenyi Zhao, Sylvain Petit, Christopher B. Kelly, John Knight
Publikováno v:
Organic Process Research & Development. 25:1701-1713
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::460b556c2b1c255389da32f969c40f58
https://doi.org/10.1021/acs.oprd.1c00300
https://doi.org/10.1021/acs.oprd.1c00300
Publikováno v:
Chemical Science
Late-stage functionalization (LSF) of heteroarenes can dramatically accelerate SAR studies by enabling the installation of functional groups that would otherwise complicate a synthetic sequence. Although heteroaryl halides and boronic esters have wel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6a25106993a7f955aa375acdbe4919
http://europepmc.org/articles/PMC8162414
http://europepmc.org/articles/PMC8162414
Autor:
Saskia M. Engle, Takisha R. Kirkner, Christopher B. Kelly, Shinsuke Shimizu, Koichi Hagiwara, Masayuki Inoue
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb4a683a29c9cb5eebf97ccc5e165048
https://doi.org/10.1002/0471264229.os096.28
https://doi.org/10.1002/0471264229.os096.28
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