127236-92-4Relevant academic research and scientific papers
Synthesis of intra annularly linked benzotriazolophane
Rajakumar, Perumal,Murali, Venghatragavan,Kalaivasan, Natarajan
, p. 1685 - 1690 (2002)
Reduction of 1,3-dialkyl benzotriazolium salts was carried out using NaH/THF. The methodology was applied for the synthesis of benzotriazolophane 2, which was intra annularly linked by p-xylenyl dibromide to give novel cyclophane 6 and reduction of benzot
Synthesis, characterization, and antimicrobial activity of lipophilic N,N′-bis-substituted triazolium salts
Fico, Dominic,Gorden, John D.,Johnson, Shanina S.,King, Lauren B.,Lin, Zi Jie,Martz, Luke,Rodriguez, Isabelle,Shelton, Kerri L.,Ta, Thong,Wilson, Julie A.
supporting information, (2021/11/30)
A series of N,N′-bis-substituted triazolium salts have been synthesized using 1H-1,2,4-triazole, 1H-1,2,3-triazole, and 1H-1,2,3-benzotriazole. Synthesized compounds were tested for their antimicrobial activities against a panel of representative ESKAPE p
SELECTIVE ALKYLATIONS OF 1,2,4-TRIAZOLE AND BENZOTRIAZOLE IN THE ABSENCE OF SOLVENT
Abenhaim, David,Diez-Barra, Enrique,Hoz, Antonio de la,Loupy, Andre,Sanchez-Migallon, Ana
, p. 793 - 802 (2007/10/02)
Alkylation of 1,2,4-triazole and benzotriazole has been performed either in basic media under solvent free phase transfer catalysis conditions or in the absence of base by conventional and microwave heating.Several parameters affecting the selectivity have been studied.In the case of triazole alkylation, microwave irradiation produces specific (non thermal) effects both on reactivity and selectivity.
Benzotriazol-1-ylmethylammonium Salts Synthesis and Reactivity
Katritzky, Alan R.,Hughes, Craig V.,Rachwal, Stanislaw
, p. 1579 - 1588 (2007/10/02)
Benzotriazol-1-ylmethylamines on treatment with alkylating agents afford benzotriazol-1-ylmethylammonium salts, also available from reactions of chloromethylbenzotriazole with tertiary amines.In deuterated solvents under basic conditions the methylene protons of these salts exchange with deuterium.At elevated temperatures, an alkyl group substituent migrated from the ammonium center to the benzotriazolyl N-3.Reactions of the salts with Grignard reagents afforded various products arising from substitution of the ammonium moiety and/or from attack on the benzotriazolyl N-3 or on the benzenoid ring.
