17646-88-7Relevant academic research and scientific papers
A facile BPO-mediated ortho -hydroxylation and benzoylation of N -alkyl anilines for synthesis of 2-benzamidophenols
Zhang, Zhi-Jing,Quan, Xue-Jing,Ren, Zhi-Hui,Wang, Yao-Yu,Guan, Zheng-Hui
supporting information, p. 3292 - 3295 (2014/07/08)
A facile benzoyl peroxide (BPO) mediated ortho-hydroxylation and benzoylation of N-alkyl anilines for the synthesis of 2-benzamidophenols has been developed. The reaction tolerates a wide range of functional groups and is a good method for the straightfor
Reduction of quinolines to 1,2,3,4-tetrahydro derivatives employing a combination of NaCNBH3 and BF3.OEt2
Srikrishna, Adusumilli,Reddy, T. Jagadeeswar,Viswajanani, Ranganathan
, p. 1631 - 1636 (2007/10/03)
A regiospecific reduction of quinolines (and 1,10-phenanthroline) into the corresponding 1,2,3,4-tetrahydro derivatives using a combination of sodium cyanoborohydride and boron trifluoride etherate in refluxing methanol is described. Under the same conditions indole and acridine reduced to the corresponding dihydroderivatives, whereas acyl group transfer from oxygen to nitrogen atom is also noticed in the case of 8-acyloxyquinolines.
