WOS: 000236916700003Six new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursors have been synthesized and characterized. These salts, in combination with palladium acetate, provide active catalysts for the cross-coupling of aryl chlorides and bromides under mild conditions in aqueous media. Copyright (c) 2006 John Wiley & Sons, Ltd
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
WOS: 000250070600001A highly effective, easy to handle and environmentally benign process for a pall...
Four bis(3,4,5,6-tetrahydropyrimidinium) chlorides (2a-d) have been prepared and characterized by co...
Six new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursors have been synthesi...
A new series of xylyl-linked bis-benzimidazolium salts were efficiently prepared using a simple prep...
WOS: 000231993000017New, sterically demanding 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (2) a...
WOS: 000225241500011Four functionalized bis(benzimidazolium) salts (2a-d) have been prepared and cha...
New, sterically demanding 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (2) as NHC precursors hav...
WOS: 000253932800017New, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic ...
WOS: 000253264500008Two benzimidazolium moieties linked by one or two xylyls (m- and p-) have been s...
WOS: 000230351300012The in situ prepared three-component system Pd(OAC)(2)-1,3-dialkylbenzimidazoliu...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
A robust palladium catalyst system supported by the hybrid ligand N-heterocyclic carbene along with ...
A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki ...
WOS: 000272605500006The reaction of 1-alkylbenzimidazole derivatives with o-/p-di(chloromethyl) benz...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
WOS: 000250070600001A highly effective, easy to handle and environmentally benign process for a pall...
Four bis(3,4,5,6-tetrahydropyrimidinium) chlorides (2a-d) have been prepared and characterized by co...
Six new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursors have been synthesi...
A new series of xylyl-linked bis-benzimidazolium salts were efficiently prepared using a simple prep...
WOS: 000231993000017New, sterically demanding 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (2) a...
WOS: 000225241500011Four functionalized bis(benzimidazolium) salts (2a-d) have been prepared and cha...
New, sterically demanding 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (2) as NHC precursors hav...
WOS: 000253932800017New, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic ...
WOS: 000253264500008Two benzimidazolium moieties linked by one or two xylyls (m- and p-) have been s...
WOS: 000230351300012The in situ prepared three-component system Pd(OAC)(2)-1,3-dialkylbenzimidazoliu...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
A robust palladium catalyst system supported by the hybrid ligand N-heterocyclic carbene along with ...
A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki ...
WOS: 000272605500006The reaction of 1-alkylbenzimidazole derivatives with o-/p-di(chloromethyl) benz...
We have previously shown that the use of ligand-free palladium employing Pd(OAc)2 as catalyst precur...
WOS: 000250070600001A highly effective, easy to handle and environmentally benign process for a pall...
Four bis(3,4,5,6-tetrahydropyrimidinium) chlorides (2a-d) have been prepared and characterized by co...