The reaction of acylium salts with dialkylcyanamides

Al‐Talib, Mahmoud; Tashtoush, Hasan

doi:10.1016/s0040-4039(00)95728-9

Cited by 10 publications

(2 citation statements)

References 10 publications

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“…[3][4][5][6][7] Al ter na tively, they can also be ob tained by re ac tions of RCONHNH2 with ei ther R2COOH or CS2 di rectly. [3][4][5][6][7] Al ter na tively, they can also be ob tained by re ac tions of RCONHNH2 with ei ther R2COOH or CS2 di rectly.…”

Section: Re Sults and Discussionmentioning

confidence: 99%

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Synthesis and Antibacterial Activities of 2‐(1‐Aryl‐5‐Methyl‐1,2,3‐triazol‐4‐yl)‐1,3,4‐Oxadiazole Derivatives

Zhang

Qiao

et al. 2002

J Chinese Chemical Soc

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Eighteen novel 2‐(1‐aryl‐5‐methyl‐1,2,3‐triazol‐4‐yl)‐1,3,4‐oxadiazole derivatives and two acylhydrazone intermediate compounds were synthesized by various pathways starting from 1‐aryl‐5‐methyl‐1,2,3‐triazol‐4‐formhydrazide (1). All products were identified by spectroscopic analysis, and 2‐(1‐aryl‐5‐methyl‐1,2,3‐triazol‐4‐yl)‐5‐benzalthio‐1,3,4‐oxadiazole was further validated by X‐ray crystallography. Results from primary antibacterial activity tests indicated that most of the compounds were effective against E. coli, P. aeruginosa, B. subtilis and S. aureus.

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Section: Re Sults and Discussionmentioning

confidence: 99%

“…[3][4] Com bining 1-aryl-5-methyl-1,2,3-triazole with sub sti tuted 1,3,4-oxadiazole is ex pected to give new com pounds with better bi o log i cal ac tiv i ties. 2 1,2,3-Triazole and re lated com pounds have attracted much at ten tion in more and more re ports due to their in dis pens able roles in both ag ri cul ture and in dus try.…”

Section: Introductionmentioning

confidence: 99%