C―H Activation
暂无分享,去创建一个
[1] T. Mei,et al. Activation of remote meta-C–H bonds assisted by an end-on template , 2012, Nature.
[2] T. Mei,et al. Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions. , 2012, Accounts of chemical research.
[3] Peter S. Thuy-Boun,et al. Ligand-accelerated cross-coupling of C(sp2)-H bonds with arylboron reagents. , 2011, Journal of the American Chemical Society.
[4] A. Edmunds,et al. Ligand-promoted C3-selective arylation of pyridines with Pd catalysts: gram-scale synthesis of (±)-preclamol. , 2011, Journal of the American Chemical Society.
[5] A. Stepan,et al. Divergent C-H functionalizations directed by sulfonamide pharmacophores: late-stage diversification as a tool for drug discovery. , 2011, Journal of the American Chemical Society.
[6] jin-quan yu,et al. Pd(II)-catalyzed carbonylation of C(sp3)-H bonds: a new entry to 1,4-dicarbonyl compounds. , 2010, Journal of the American Chemical Society.
[7] jin-quan yu,et al. Pd(II)-catalyzed hydroxyl-directed C-H activation/C-O cyclization: expedient construction of dihydrobenzofurans. , 2010, Journal of the American Chemical Society.
[8] jin-quan yu,et al. Ligand-Enabled Reactivity and Selectivity in a Synthetically Versatile Aryl C–H Olefination , 2010, Science.