1159978-92-3Relevant academic research and scientific papers
A two-step, single pot procedure for the synthesis of substituted dihydropyrazolo-pyrimidines
Zimmerman, Jake R.,Myers, Brian J.,Bouhall, Samantha,McCarthy, Allison,Johntony, Olivia,Manpadi, Madhuri
supporting information, p. 936 - 940 (2015/03/03)
In this study, we report a two-step, one pot tandem microwave-assisted reaction of 3-formylchromones with aminopyrazoles followed by a tin-free radical addition. A library of alkyl substituted dihydropyrazolopyrimidines was prepared using this new process.
In vitro cytotoxicity of hydrazones, pyrazoles, pyrazolo-pyrimidines, and pyrazolo-pyridine synthesized from 6-substituted 3-formylchromones
Galarraga, Elier,Urdaneta, Neudo,Gutierrez, Keily J.,Herrera, Julio C.
, p. 305 - 310 (2015/05/20)
Pyrazoles 4a-f, hydrazones 5a-c and 6a-c, pyrazolo[1,5-a]pyrimidines 7a, b, and pyrazolo[3,4-b]pyridine 8 were prepared in good yields (80-95%) from the reaction of 6-substituted (H, Me, F) 3-formylchromones 1a-c with N-substituted hydrazines 2a-c and ami
A two-step, single pot procedure for the synthesis of substituted dihydropyrazolo-pyrimidines
Zimmerman, Jake R.,Myers, Brian J.,Bouhall, Samantha,McCarthy, Allison,Johntony, Olivia,Manpadi, Madhuri
supporting information, p. 936 - 940 (2014/02/14)
In this study, we report a two-step, one pot tandem microwave-assisted reaction of 3-formylchromones with aminopyrazoles followed by a tin-free radical addition. A library of alkyl substituted dihydropyrazolopyrimidines was prepared using this new process.
