Water-soluble palladacycles containing hydroxymethyl groups: synthesis, crystal structures and use as catalysts for amination and Suzuki coupling of reactions
作者:Xin Han、Hong-Mei Li、Chen Xu、Zhi-Qiang Xiao、Zhi-Qiang Wang、Wei-Jun Fu、Xin-Qi Hao、Mao-Ping Song
DOI:10.1007/s11243-016-0036-5
日期:2016.5
2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl(Sphos)]-palladacycles containing hydroxymethyl groups 2–3 were prepared by cyclopalladation and chloride bridge-splitting reactions. The complexes were characterized by elemental analysis, ESI–MS and NMR. In addition, single-crystal X-ray analysis reveals that they have one-dimensional lamellar structures involving intermolecular hydrogen bonds and π–π interactions
Coupling reactions with haloaromatic amines and alcohols for a practical synthetic route to 2-substituted aminophenyl and hydroxyphenyl pyridines
作者:Seung-Hoi Kim、Reuben D. Rieke
DOI:10.1016/j.tetlet.2009.09.160
日期:2009.12
A practical syntheticroute to 2-substituted aminophenyl and hydroxyphenyl pyridines has been developed. It has been accomplished by the cross-coupling reactions of readily available 2-pyridylzinc bromides with haloaromatic amines and alcohols under mild conditions.
2-Pyridyl and 3-pyridylzinc bromides: direct preparation and coupling reaction
作者:Seung-Hoi Kim、Reuben D. Rieke
DOI:10.1016/j.tet.2010.02.061
日期:2010.4
A facile synthetic approach to the direct preparation of 2-pyridyl and 3-pyridylzinc bromides has been demonstrated usingRieke zinc with 2-bromopyridine and 3-bromopyridine, respectively. A variety of different electrophiles have been coupled with the resulting organozinc reagents to give the corresponding cross-coupling products in moderate to good yields.