
![]() |
|||||||||||||
WJPR Citation
|
| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
AN EFFICIENT SUZUKI REACTION USING A NEW BENZOTHIAZOLE/ PD(II) SPECIES AS CATALYST IN AQUEOUS MEDIA
Mayank J. Mamtora, Javed G. Mahetar, Juvansinh J. Jadeja, Rohit B. Manawar, Manish K. Shah*
Abstract N,N,O-donating ligand was prepared from the condensation of 2- amino benzothiazole with various aromatic aldehyde. Metal complex of this ligand is neither air nor moisture sensitive. The effects of varying solvents, bases, and ligand/copper ratio on the performance of the coupling reaction were investigated. This method is a very simple, efficient and mild protocol for the cross-coupling of aryl bromides with arylboronic acids, and the reactions proceeded effortlessly in excellent yields within short reaction times. All reactions are carried out in anhydrous condition. Keywords: N,N,O-donating ligand was prepared from the condensation of 2- amino benzothiazole with various aromatic aldehyde. Metal complex of this ligand is neither air nor moisture sensitive. The effects of varying solvents, bases, and ligand/copper ratio on the p [Full Text Article] [Download Certificate] |
