Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dmitry P. Lubov"'
Publikováno v:
Organic Letters. 25:1359-1363
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5daab19bc7c295db9da0368ee7c6c923
https://doi.org/10.1021/acs.orglett.2c04371
https://doi.org/10.1021/acs.orglett.2c04371
Autor:
Dmitry P. Lubov, Konstantin P. Bryliakov, Anna A. Bryliakova, Denis G. Samsonenko, Dmitriy G. Sheven, Evgenii P. Talsi
Publikováno v:
ChemCatChem. 13:5109-5120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18779e1ce826753de3149288fdaeb3ea
https://doi.org/10.1002/cctc.202101345
https://doi.org/10.1002/cctc.202101345
Publikováno v:
Russian Chemical Reviews. 89:587-628
The development of methods for the selective oxidation of C–H groups of organic compounds resulting in C–O bond formation is a challenging problem in modern synthetic organic chemistry. Versatile methods for the oxofunctionalization of these grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7de6a3da6307680f783f5b5485593de7
https://doi.org/10.1070/rcr4918
https://doi.org/10.1070/rcr4918
Autor:
Tatyana V. Rybalova, Oleg Y. Lyakin, Konstantin P. Bryliakov, Denis G. Samsonenko, Dmitry P. Lubov, Evgenii P. Talsi
Publikováno v:
Dalton Transactions. 49:11150-11156
Four palladium(ii) complexes with tripodal ligands of the tpa family (tpa = tris(2-pyridylmethyl)amine) have been synthesized and X-ray characterized. These complexes efficiently catalyze benzylic C-H oxidation of various substrates with peracetic ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf29678e374d1f3aeb7059c5e04def02
https://doi.org/10.1039/d0dt02247k
https://doi.org/10.1039/d0dt02247k
Autor:
Oleg Y. Lyakin, Evgenii P. Talsi, Konstantin P. Bryliakov, Alexandra M. Zima, Dmitry P. Lubov
Publikováno v:
Molecular Catalysis. 493:111039
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ebf4093153ddeba681d042a5293b99e
https://doi.org/10.1016/j.mcat.2020.111039
https://doi.org/10.1016/j.mcat.2020.111039
Autor:
Evgenii P. Talsi, Dmitry P. Lubov, Alexandra M. Zima, Oleg Y. Lyakin, Konstantin P. Bryliakov
Publikováno v:
Molecular Catalysis. 483:110708
Direct data on the reactivity of the nonheme iron(V)-oxo intermediates toward substituted benzenes at −70 °C have been obtained. The intermediates are generated in the catalyst systems 1/CH3CO3H/RCOOH (1 = [(PDP*)2FeIII2(μ-OH)2](OTf)4, PDP* = N,N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd37867a2f4e404e923f7069885abe37
https://doi.org/10.1016/j.mcat.2019.110708
https://doi.org/10.1016/j.mcat.2019.110708