Zobrazeno 1 - 10
of 34
pro vyhledávání: '"M. Ramu Yadav"'
Publikováno v:
The Journal of Organic Chemistry. 88:5652-5660
Autor:
Suvajit, Koley, Kaylee T, Cayton, Gisela A, González-Montiel, M Ramu, Yadav, Douglas L, Orsi, Andrew J, Intelli, Paul Ha-Yeon, Cheong, Ryan A, Altman
Publikováno v:
The Journal of organic chemistry. 87(16)
A Cu-based catalyst system convergently couples
Autor:
Suvajit Koley, Kaylee T. Cayton, Gisela A. González-Montiel, M. Ramu Yadav, Douglas L. Orsi, Andrew J. Intelli, Paul Ha-Yeon Cheong, Ryan A. Altman
Publikováno v:
The Journal of Organic Chemistry. 87:10710-10725
Autor:
Suvajit Koley, Kaylee Cayton, Douglas L. Orsi, Ryan A. Altman, Gisela A. González-Montiel, M. Ramu Yadav, Paul H-Y Cheong
A Cu-based catalyst system convergently couples gem-difluoroalkenes with phenols under aerobic conditions to deliver α,α-difluorinated-α-phenoxy ketones, an unstudied hybrid fluorinated functional group. Composed of α,α-difluorinated ketone and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cecc6f9aefba24de5222b347b4fb65b
https://doi.org/10.33774/chemrxiv-2021-w4mv5
https://doi.org/10.33774/chemrxiv-2021-w4mv5
Autor:
M. Ramu Yadav, Ruchi Sharma
Publikováno v:
Organicbiomolecular chemistry. 19(25)
Decarboxylative coupling reactions using readily available (hetero)aryl carboxylic acids are a highly efficient approach for the formation of new C-C and C-X bonds. These decarboxylative coupling reactions eliminate CO2 as a by-product, resulting in
Publikováno v:
Tetrahedron. 75:4325-4336
Gem-difluoroalkenes are an easily accessed fluorinated functional group, and a useful intermediate for elaborating into more complex fluorinated compounds. Currently, most functionalization reactions of gem-difluoroalkenes, with or without a transiti
Publikováno v:
Tetrahedron
Gem-difluoroalkenes are an easily accessed fluorinated functional group, and a useful intermediate for elaborating into more complex fluorinated compounds. Currently, most functionalization reactions of gem-difluoroalkenes, with or without a transiti
Publikováno v:
Organic Letters. 20:1655-1658
The Pd-catalyzed reductive denitration of nitroarenes has been achieved via a direct cleavage of the C–NO2 bonds. The catalytic conditions reported exhibit a broad substrate scope and good functional-group compatibility. Notably, the use of inexpen
Autor:
Myuto Kashihara, Masahiro Nagaoka, Takanori Miyazaki, Rong-Lin Zhong, Yoshiaki Nakao, M. Ramu Yadav, Shigeyoshi Sakaki
Publikováno v:
Journal of the American Chemical Society. 139:9423-9426
Synthesis of biaryls via the Suzuki–Miyaura coupling (SMC) reaction using nitroarenes as an electrophilic coupling partners is described. Mechanistic studies have revealed that the catalytic cycle of this reaction is initiated by the cleavage of th
Autor:
Shigeyoshi Sakaki, Myuto Kashihara, Takanori Miyazaki, Yoshiaki Nakao, Masahiro Nagaoka, Rong-Lin Zhong, M. Ramu Yadav
Publikováno v:
Journal of the American Chemical Society. 140(28)