Journal
RSC ADVANCES
Volume 12, Issue 44, Pages 28862-28866Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ra05230j
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Funding
- Ministry of Science and Technology of Taiwan [MOST 110-2113-M-110-014, MOST 111-2113-M-110006]
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The catalytic activity of [(Ph2P-o-C6H4)(2)N]PdCl in aerobic aqueous Suzuki couplings is described. The molecular catalyst can efficiently cross-couple arylboronic acids with various electronically activated, unactivated, and deactivated aryl iodides, bromides, and chlorides in aqueous solutions under aerobic conditions, yielding biphenyl derivatives without the need for amphiphiles, even in the presence of an excess of mercury.
The catalytic activity of [(Ph2P-o-C6H4)(2)N]PdCl in aerobic aqueous Suzuki couplings is described. Though hydrophobic, this molecular catalyst is competent in cross-coupling reactions of arylboronic acids with a variety of electronically activated, unactivated, and deactivated aryl iodides, bromides, and chlorides upon heating in aqueous solutions under aerobic conditions to give biphenyl derivatives without the necessity of amphiphiles even in the presence of an excess amount of mercury.
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