Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Samantha Rohe"'
Publikováno v:
The Journal of Organic Chemistry. 85:2806-2813
While attempting to synthesize biaryl ethers we discovered the inadvertent formation of a methylsulfoxylmethyl ether byproduct. Formation of this unexpected byproduct presented an opportunity to streamline the synthesis of methylsulfoxylmethyl ethers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131a95ac1e7e7eae5febf2534404281e
https://doi.org/10.1021/acs.joc.9b03237
https://doi.org/10.1021/acs.joc.9b03237
Publikováno v:
Angewandte Chemie. 130:15890-15895
The selective functionalization of chemically inert C-H bonds remains to be fully realized in achieving organic transformations that are redox-neutral, waste-limiting, and atom-economical. The catalytic generation of chlorine atoms from chloride ions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e5c239bf566b365c272864b17ea14cb
https://doi.org/10.1002/ange.201810187
https://doi.org/10.1002/ange.201810187
Publikováno v:
Catalysis Science & Technology. 8:6019-6028
In this minireview, recent developments in the field of photoredox catalysis and the applications of mono and binuclear Au(I) complexes in organic transformations are discussed. More specifically, a brief introduction of the photophysical properties
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::307cbba65d547f05540f91fd724d5267
https://doi.org/10.1039/c8cy01765d
https://doi.org/10.1039/c8cy01765d
Autor:
W. Zhang, J. C. Tellis, M. Rueping, A. S. K. Hashmi, S.-g. Lee, G. A. Molander, Louis Barriault, K. Muralirajan, D. N. Primer, O. Riant, U B. Kim, J. Wang, X. Huo, R. He, Samantha Rohe, V. W. Bhoyare, Y. Nakao, N. T. Patil, M. Zidan, A. G. Tathe, S. K. Rout, X. Shi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41f8308f2ababaf2f4127d5f90bc7840
https://doi.org/10.1055/b-006-164899
https://doi.org/10.1055/b-006-164899
Publikováno v:
Dual Catalysis in Organic Synthesis 1 ISBN: 9783132429765
Dual Catalysis in Organic Synthesis 1
Dual Catalysis in Organic Synthesis 1
The use of gold catalysts in classical two-electron cross-couplings is notoriously impractical due to the high oxidation potential of gold(I)/gold(III) [e.g., E0 (AuI/AuIII) = +1.36 V]. However, when used in tandem with photocatalysts, the gold cente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::260c2470f2134a5ad2e3877b2371a1e1
https://doi.org/10.1055/sos-sd-231-00189
https://doi.org/10.1055/sos-sd-231-00189
Publikováno v:
Synlett. 28:289-305
Light-mediated photoredox transformations have become commonplace in contemporary catalysis research and design. Excited-state redox catalysts trigger photoinduced electron transfers (PET) through oxidative or reductive quenching modes, allowing acce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2e02d64d12dba28a69c43ff1ee57599
https://doi.org/10.1055/s-0036-1588644
https://doi.org/10.1055/s-0036-1588644
Publikováno v:
Angewandte Chemie International Edition. 57
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb32fe2fba8a348efdb85339de5e87b2
https://doi.org/10.1002/anie.201884861
https://doi.org/10.1002/anie.201884861
Publikováno v:
Angewandte Chemie. 130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39672c66857aab881d2a8c7f1d8d195f
https://doi.org/10.1002/ange.201884861
https://doi.org/10.1002/ange.201884861
Publikováno v:
The Journal of organic chemistry. 83(17)
Isonitriles have excellent electronic compatibility to react with free radicals. Recently, photoredox catalysis has emerged as a powerful tool for the construction of C–C bonds with few protocols for alkylative heterocycle synthesis through isonitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62a2781eab8681e7c97075b5c782a3ab
https://pubmed.ncbi.nlm.nih.gov/29979602
https://pubmed.ncbi.nlm.nih.gov/29979602