104499-04-9Relevant articles and documents
An Unexpected Double Cycloaddition of Triazolopyrimidine N-Ylide with Activated Acetylenes and Alkenes
Hori, Mikio,Kataoka, Tadashi,Shimizu, Hiroshi,Imai, Eiji,Tanaka, Kiyomi,et al.
, p. 2531 - 2538 (2007/10/02)
The reaction of 5,7-dimethyl-triazolopyrimidinio-3-phenacylide (5) with activated acetylenes gave 1 : 2 adducts of ylide-R-CC-R.The structures of the products were determined as 3,3a-dihydropyrazolopyrimidine derivatives (7) by hyd
Generation of triazolopyrimidine N-Ylides and Their Ring Transformation Reactions
Hori, Mikio,Tanaka, Kiyomi,Kataoka, Tadashi,Shimizu, Hiroshi,Imai, Eiji,et al.
, p. 2333 - 2336 (2007/10/02)
Triazolopyrimidine (1) has been alkylated at the N(3)-position by treatment with alkyl halides in refluxing dry acetone.The ylides (3) were generated in situ from the iminium salts (2) and 1 equiv. of triethylamine.Thermolysis of the ylides