Zobrazeno 1 - 10
of 24
pro vyhledávání: '"A. S. Burukin"'
Publikováno v:
Russian Chemical Bulletin. 71:1656-1661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83ac996747311c1157cd2d089f0af39f
https://doi.org/10.1007/s11172-022-3575-2
https://doi.org/10.1007/s11172-022-3575-2
Publikováno v:
Russian Chemical Bulletin. 71:169-172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::105132d7c23e374e9450e5fddbdb7185
https://doi.org/10.1007/s11172-022-3392-7
https://doi.org/10.1007/s11172-022-3392-7
Publikováno v:
Mendeleev Communications. 31:400-402
Screening of four Buchwald ligands for the cross-coupling of isomeric di-, tri- and tetrachlorobenzenes with arylboronic acids revealed that good yields of exhaustive substitution can be best provided by 2-dicyclohexylphosphino-2′-(dimethylamino) b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59d68a6443621eefaadd3cf8963aeed9
https://doi.org/10.1016/j.mencom.2021.05.039
https://doi.org/10.1016/j.mencom.2021.05.039
Publikováno v:
Russian Chemical Reviews. 76:885-916
Methods for the replacement of chlorine atoms in polychloroarenes upon treatment with various reagents are surveyed. Considerable attention is given to catalytic methods and elucidation of the structure–reactivity relationships for polychloroarenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bb43a33c44112a60997febc34788460
https://doi.org/10.1070/rc2007v076n10abeh003724
https://doi.org/10.1070/rc2007v076n10abeh003724
Publikováno v:
Russian Chemical Bulletin. 55:118-122
The Suzuki cross-coupling with phenylboronic acid in the presence of the Pd(OAc)2/K3PO4/DMF catalytic system was successful for aryl bromides and somewhat poorer for aryl chlorides. Addition of 1,3-bis(tetrazol-1-yl)benzene or its analogs lowered the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31e0079f92ce0ad8a8814eb7096a2007
https://doi.org/10.1007/s11172-006-0224-0
https://doi.org/10.1007/s11172-006-0224-0
Publikováno v:
Russian Chemical Bulletin. 54:970-974
Hexachlorobenzene and 1,2,4,5-tetrachlorobenzene react with phenylboronic acid by a C—C cross-coupling mechanism with a Pd(dba)2/P(But)3 system (dba is dibenzylideneacetone) or palladium-azole complexes as catalysts, or with organozinc compounds in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c8f3003ab94690e54b62b1222ba7108
https://doi.org/10.1007/s11172-005-0342-0
https://doi.org/10.1007/s11172-005-0342-0
Autor:
E. A. Mistryukov, Andrei A. Vasil'ev, N. L. Merkulova, S. G. Zlotin, A. S. Burukin, Alexander O. Chizhov
Publikováno v:
Russian Chemical Bulletin. 56:1467-1469
The reactions of di-, tetra-, and hexachlorobenzenes with phenylboronic acid in the presence of [Pd]-imidazolium salt-base as catalytic systems afford cross-coupling products in moderate yields. The highest conversions are attained when imidazolium s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ace91fedd30eeb4c494ed64941e941cc
https://doi.org/10.1007/s11172-007-0224-8
https://doi.org/10.1007/s11172-007-0224-8
Autor:
N. L. Merkulova, S. G. Zlotin, E. A. Mistryukov, Alexander O. Chizhov, Andrei A. Vasil'ev, A. S. Burukin
Publikováno v:
ChemInform. 39
The reactions of di-, tetra-, and hexachlorobenzenes with phenylboronic acid in the presence of [Pd]-imidazolium salt-base as catalytic systems afford cross-coupling products in moderate yields. The highest conversions are attained when imidazolium s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfcbb7cdcdbe65328321665f45ddb8f5
https://doi.org/10.1002/chin.200823089
https://doi.org/10.1002/chin.200823089
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02587df72d5a33ab71cfbfecc0b25990
https://doi.org/10.1002/chin.200813260
https://doi.org/10.1002/chin.200813260
Publikováno v:
ChemInform. 37
Polychloroaromatic compounds lithiated by BunLi in THF react with several electrophilic agents of which aldehydes and epoxides seem to be the most promising from the preparative point of view.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690eaa8362100a0756376f62358c17f1
https://doi.org/10.1002/chin.200618046
https://doi.org/10.1002/chin.200618046