Korbukh, I. A. et al. published their research in Zhurnal Organicheskoi Khimii in 1973 | CAS: 49834-67-5

1H-Pyrazolo[3,4-b]pyridin-4-ol (cas: 49834-67-5) belongs to pyrazole derivatives. The strategies for the synthesis of pyrazoles generally can be applied for the construction of indazoles. Pyrazoles can be selectively lithiated at different carbons and subsequently react with electrophiles depending on the substitution patterns.Product Details of 49834-67-5

Glycosides of pyrazole and condensed pyrazole heterocycles. II. Synthesis of pyrazolo-[3,4-b]pyridine glycosides was written by Korbukh, I. A.;Blanko, F. F.;Preobrazhenskaya, M. N.;Dorn, H.;Kondakova, N. G.;Sukhova, T. I.;Kostyuchenko, N. P.. And the article was included in Zhurnal Organicheskoi Khimii in 1973.Product Details of 49834-67-5 The following contents are mentioned in the article:

β-D-Ribofuranosylpyrazolo[3,4-b]pyridines (I; R1 = Cl, H2NNH, Me2N, H2N, MeS) were obtained by condensation of the appropriate pyrazolo[3,4-b]pyridines with acyl derivatives of saccharides, followed by deacylation and appropriate substitution reactions. Addnl. 1-β-D-glucopyranosyl-4-chloropyrazolo[3,4-b]pyridine was prepared This study involved multiple reactions and reactants, such as 1H-Pyrazolo[3,4-b]pyridin-4-ol (cas: 49834-67-5Product Details of 49834-67-5).

1H-Pyrazolo[3,4-b]pyridin-4-ol (cas: 49834-67-5) belongs to pyrazole derivatives. The strategies for the synthesis of pyrazoles generally can be applied for the construction of indazoles. Pyrazoles can be selectively lithiated at different carbons and subsequently react with electrophiles depending on the substitution patterns.Product Details of 49834-67-5

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics