Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ramon, Arora"'
Autor:
E. Ali McKnight, Ramon Arora, Ekadashi Pradhan, Yuriko H. Fujisato, Ayonitemi J. Ajayi, Mark Lautens, Tao Zeng, Christine M. Le
Publikováno v:
Journal of the American Chemical Society. 145:11012-11018
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abe6cb5b04d442ad959f0f48e0405f93
https://doi.org/10.1021/jacs.3c03982
https://doi.org/10.1021/jacs.3c03982
Publikováno v:
ACS Catalysis. 13:6562-6567
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05eb3745d2b28afbbb5bb7a5716de672
https://doi.org/10.1021/acscatal.3c01055
https://doi.org/10.1021/acscatal.3c01055
Publikováno v:
Journal of the American Chemical Society. 144:20554-20560
A Pd(0)/blue light catalyzed carboiodination reaction is reported. A simple, air-stable catalytic system, utilizing [Pd(allyl)Cl]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54e8bd50c5dfb2fcc93ea56a73b8cf0f
https://doi.org/10.1021/jacs.2c09716
https://doi.org/10.1021/jacs.2c09716
Autor:
E. Ali McKnight, Ramon Arora, Ekadashi Pradhan, Yuriko H. Fujisato, Ayonitemi J. Ajayi, Mark Lautens, Tao Zeng, Christine M. Le
A BF3-catalyzed atom-economical fluorocarbamoylation reaction of alkyne-tethered carbamoyl fluorides is reported. The catalyst acts as both a fluoride source and Lewis acid activator, enabling the formal insertion of alkynes into strong C–F bonds t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13435e67bc31618b2b3d210b7debdd8d
https://doi.org/10.26434/chemrxiv-2022-464nx-v2
https://doi.org/10.26434/chemrxiv-2022-464nx-v2
Autor:
E. Ali McKnight, Ramon Arora, Yuriko H. Fujisato, Ayonitemi J. Ajayi, Mark Lautens, Christine M. Le
A BF3-catalyzed atom-economical fluorocarbamoylation reaction of alkyne-tethered carbamoyl fluorides is reported. The catalyst acts as both a fluoride source and Lewis acid activator, enabling the formal insertion of alkynes into strong C–F bonds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcfeb46dc48085e20abe75167183e58a
https://doi.org/10.26434/chemrxiv-2022-464nx
https://doi.org/10.26434/chemrxiv-2022-464nx
Publikováno v:
Organic Letters. 23:7540-7544
The reaction of alkene-tethered trifluoroacetimidoyl chlorides with trialkyl phosphites furnishes 1-amino-2,2,2-trifluoroalkylphosphonates. The products were generated in moderate to good yields, and the scalability of this process was showcased. Par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18b612897fc9cae1c61a4d8bf16e78c6
https://doi.org/10.1021/acs.orglett.1c02750
https://doi.org/10.1021/acs.orglett.1c02750
Publikováno v:
Angewandte Chemie. 133:20393-20398
An enantioselective consecutive cyclization/coupling process, catalyzed by palladium is reported. Stereoinduction arises from an enantioselective carbopalladation, generating an intermediate which promotes a nucleopalladation step. The dual cyclizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b5e36a9120d03d6918a1cb213167472
https://doi.org/10.1002/ange.202106518
https://doi.org/10.1002/ange.202106518
Publikováno v:
Angewandte Chemie (International ed. in English). 60(37)
An enantioselective consecutive cyclization/coupling process, catalyzed by palladium is reported. Stereoinduction arises from an enantioselective carbopalladation, generating an intermediate which promotes a nucleopalladation step. The dual cyclizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b74fa9fbbe4aae8b8a8766824254e3fd
https://pubmed.ncbi.nlm.nih.gov/34240542
https://pubmed.ncbi.nlm.nih.gov/34240542