81810-81-3Relevant academic research and scientific papers
Telescoped Synthesis of 2-Acyl-1-aryl-1,2-dihydroisoquinolines and Their Inhibition of the Transcription Factor NF-κB
Chung, Tsai-Wen,Hung, Yi-Tzu,Thikekar, Tushar,Paike, Vijaykumar V.,Lo, Fu Yuan,Tsai, Pei-Hua,Liang, Mei-Chih,Sun, Chung-Ming
, p. 442 - 451 (2015)
(Chemical Equation Presented). A sequential single-flask multicomponent reactions is highly effective for the synthesis of 1,2-dihydroisoquinolines through amidealkylation from intermediate N-acylisoquinolinium salts under mild conditions. N-Acylisoquinol
DUAL REACTIVITIES OF 1,2-DISUBSTITUTED DIHYDRO-N-HETEROAROMATIC SYSTEMS. 3. ELECTROCHEMICAL AROMATIZATION OF SUBSTITUTED N-ACYLDIHYDROPYRIDINES AND IMIDAZOLES
Sosonkin, I. I.,Sheinkman, A. K.,Skorobogatova, Z. M.,Strogov, G. N.,Ikher, T. P.
, p. 272 - 276 (2007/10/02)
The principal pathway in the fragmentation of the cation radicals of N-acyl-α(γ)-substituted 1,4-dihydropyridines and 1,2-dihydroisoquinolines, as well as 1,2-dihydroimidazoles and 1,2-dihydrobenzimidazoles, that are formed in the electrochemical oxidation of the indicated N-acyldihydro-N-heteroaromatic systems is the loss of a proton and the subsequent loss of another electron or detachment of an N-acyl residue in the form of a cation and subsequent detachment of an electron to give the corresponding γ(α)-substituted heteroaromatic cations.
