A highly effective, easy to handle and environmentally benign process for a palladium mediated Heck reaction was developed. The in situ prepared 3-component system, Pd(OAc)2 / 1,3-dialkylbenzimidazolium chlorides (LHX = 1a-g) and Cs2CO3, catalyzes quantitatively the Heck coupling of aryl bromides under mild conditions in aqueous media
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
WOS: 000232045500034A highly effective, easy to handle, and environmentally benign process for palla...
[[abstract]]A new phosphine−imidazolium salt, L·HBr (1, L = (1-ethylenediphenylphosphino-3-(mesityl)...
WOS: 000250070600001A highly effective, easy to handle and environmentally benign process for a pall...
A palladium/imidazolium chloride system has been used to catalyze the Heck reaction. The combination...
PubMed ID: 20335935An efficient and stereoselective catalytic system for the Heck cross coupling rea...
WOS: 000230351300012The in situ prepared three-component system Pd(OAC)(2)-1,3-dialkylbenzimidazoliu...
A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki ...
WOS: 000253932800017New, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic ...
WOS: 000236916700003Six new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursor...
Six new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursors have been synthesi...
WOS: 000269723700008The oligoether-substituted (CH3(OCH2CH2)(n)-; n = 1, 2 or 3) benzimidazolium bro...
WOS: 000224013200001From readily available starting compounds, six functionalized 1,3-dialkylbenzimi...
A new phosphine-imidazolium salt, L.HBr (1 . HBR = (1-ethylenediphenylphosphino-3-(mesityl))imidazol...
Palladium-catalyzed cross-coupling reactions have emerged as one of the most versatile tools in orga...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
WOS: 000232045500034A highly effective, easy to handle, and environmentally benign process for palla...
[[abstract]]A new phosphine−imidazolium salt, L·HBr (1, L = (1-ethylenediphenylphosphino-3-(mesityl)...
WOS: 000250070600001A highly effective, easy to handle and environmentally benign process for a pall...
A palladium/imidazolium chloride system has been used to catalyze the Heck reaction. The combination...
PubMed ID: 20335935An efficient and stereoselective catalytic system for the Heck cross coupling rea...
WOS: 000230351300012The in situ prepared three-component system Pd(OAC)(2)-1,3-dialkylbenzimidazoliu...
A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki ...
WOS: 000253932800017New, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic ...
WOS: 000236916700003Six new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursor...
Six new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursors have been synthesi...
WOS: 000269723700008The oligoether-substituted (CH3(OCH2CH2)(n)-; n = 1, 2 or 3) benzimidazolium bro...
WOS: 000224013200001From readily available starting compounds, six functionalized 1,3-dialkylbenzimi...
A new phosphine-imidazolium salt, L.HBr (1 . HBR = (1-ethylenediphenylphosphino-3-(mesityl))imidazol...
Palladium-catalyzed cross-coupling reactions have emerged as one of the most versatile tools in orga...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
WOS: 000232045500034A highly effective, easy to handle, and environmentally benign process for palla...
[[abstract]]A new phosphine−imidazolium salt, L·HBr (1, L = (1-ethylenediphenylphosphino-3-(mesityl)...