17330-10-8Relevant academic research and scientific papers
1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N1 and N2 substituted triazoles
Dhuri, Sundar N.,Harmalkar, Sarvesh S.,Maddani, Mahagundappa R.,P., Kavyashree,Rai, Vishakha
supporting information, p. 345 - 351 (2022/01/20)
The regioselective syntheses of N1 and N2 substituted triazoles through a 1,6-addition reaction of 1,2,3-NH triazoles to p-quinone methide were achieved under mild reaction conditions. The present reactions showed superior results in terms of selectivity, mild reaction conditions, short reaction time and broad substrate scope with good functional-group compatibility. Considering the high synthetic value of N1- and N2-substituted compounds and p-QM related research, the present strategy will greatly benefit researchers in various fields.
AMINOMETHYLATION OF 2,6-DI-TERT-BUTYLPHENOL BY THE AMINALS OF AROMATIC ALDEHYDES
Komissarov, V. N.,Ukhin, L. Yu.
, p. 2326 - 2328 (2007/10/02)
The reaction of 2,6-di-tert-butylphenol with the aminals of aromatic aldehydes gave its 4-aryldialkylaminomethyl derivatives.
