Methods for the synthesis of 1H-pyrazolo[3,4-b]pyridine derivatives

AV Smolobochkin, AS Gazizov, AR Garifzyanov… - Russian Chemical …, 2022 - Springer
This review covers and summarizes comprehensive data reported within the period from
2017 to 2021 on the synthetic strategies and approaches to 1 H-pyrazolo [3, 4-b] pyridine …

Phospha-Michael addition of biphenylphosphine oxide to chalcones and α, β-unsaturated esters using the organocatalyst 1, 1-diaminobenzalazine

K Mehta, AA Wani, PV Bharatam - Tetrahedron Letters, 2023 - Elsevier
The phospha-Michael addition (PMA) to many Michael acceptors like nitro-olefins, cyclic
enones is well known. Chalcones and α, β-unsaturated esters are rarely employed in PMA …

Process Development for a 1H-Indazole Synthesis Using an Intramolecular Ullmann-Type Reaction

JI Day, KN Allen-Moyer, KP Cole - The Journal of Organic …, 2023 - ACS Publications
Within the scope of develo** a new route to an active pharmaceutical ingredient
intermediate, we had need of a fluorinated indazole. Although an established route was in …

1, 1-Diaminoazines as organocatalysts in phospha-Michael addition reactions

AA Wani, SS Chourasiya, D Kathuria… - Chemical …, 2021 - pubs.rsc.org
1, 1-Diaminoazines can act as effective organocatalysts for the formation of phosphorus–
carbon bonds between biphenylphosphine oxide and an activated alkene (Michael …

An NNN Pd (ii) pincer complex with 1, 1-diaminoazine: a versatile catalyst for acceptorless dehydrogenative coupling reactions

AA Wani, SM Bhujbal, D Sherpa, D Kathuria… - Organic & …, 2025 - pubs.rsc.org
An azine-based, non-palindromic, neutral NNN-pincer ligand was synthesised in a single
step with an yield of 85%. The palladation of the ligand, using Pd (OAc) 2, was performed in …

Cobalt‐Promoted Para C─H Amination of 3‐Acetyl Substituted Nitroarenes with Arylhydrazines

DK Nguyen, GTH Tran, TT Nguyen - ChemistrySelect, 2024 - Wiley Online Library
We report a method to furnish substituted 1H‐indazoles via a coupling of 3‐acetyl
substituted nitroarenes and arylhydrazines. Reactions progressed in the presence of cobalt …

Efficient approach to 1, 1′-bisindoles via copper (i)-catalyzed double domino reaction

AK Bauer, J Conrad, U Beifuss - Organic & Biomolecular Chemistry, 2023 - pubs.rsc.org
A highly efficient copper (I)-catalyzed approach for the synthesis of 1, 1′-bisindoles that is
based on the formation of four bonds in one step has been developed. The unprecedented …

Copper (I) Catalysed Tandem C− C and C− N Bond Cleavage of N‐Fused Imidazoles towards the Synthesis of N‐pyridinylamides

F Ahmad Sofi, MH Masoodi, M Ovais Dar… - …, 2023 - Wiley Online Library
Copper (I) catalysed oxidative conversion of imidazopyridines into N‐pyridinylamides has
been achieved via tandem C− C and C− N bond cleavages under oxidative reaction …

Synthesis of Polyfunctional Indazoles via Novel Rearrangement of Isatin Derivatives

E Bezsonova, V Tafeenko, S Sosonyuk… - Asian Journal of …, 2025 - Wiley Online Library
In this work we present a new method for indazole synthesis through the unexpected
rearrangement of various 7‐nitroisatins during the reaction with hydrazine hydrate. The new …

Tailor‐Made Pyrazolopyridines and Fused Pyrazolopyridines: Recent Updates toward Sustainable Synthesis

M Alam Mondal, R Ghosh - ChemistrySelect, 2024 - Wiley Online Library
Over the last three decades, owing to labour cost, time and especially environmental issues,
one‐pot synthesis of heterocyclic compounds involving tandem or multicomponent …