A3 Coupling Reaction in the Synthesis of Heterocyclic Compounds
Y Volkova, S Baranin, I Zavarzin - Advanced Synthesis & …, 2021 - Wiley Online Library
In recent years, the transition‐metal catalyzed three‐component coupling of an aldehyde, an
alkyne and an amine, commonly called A3 coupling has become a powerful tool in organic …
alkyne and an amine, commonly called A3 coupling has become a powerful tool in organic …
Recent Advances in the A3 Coupling Reactions and their Applications
Propargylamines are an important class of organic compounds that have been widely used
as building blocks for the synthesis of various kinds of chemically and biologically relevant …
as building blocks for the synthesis of various kinds of chemically and biologically relevant …
Flow synthesis approaches to privileged scaffolds–recent routes reviewed for green and sustainable aspects
AI Alfano, M Brindisi, H Lange - Green Chemistry, 2021 - pubs.rsc.org
Privileged scaffolds as starting points toward biologically active molecules represent a
neuralgic point in drug discovery. The ability of synthetic chemists concerned with their …
neuralgic point in drug discovery. The ability of synthetic chemists concerned with their …
Recent Advances in Domino Synthesis of Fused Polycyclic N‐Heterocycles Based on Intramolecular Alkyne Hydroamination under Copper Catalysis
Z Jin, G Shen, X Lv - Chinese Journal of Chemistry, 2023 - Wiley Online Library
Comprehensive Summary Fused polycyclic N‐heterocycles are very important scaffolds in
biomedicinal chemistry and materials science. Intramolecular alkyne hydroamination is a …
biomedicinal chemistry and materials science. Intramolecular alkyne hydroamination is a …
[HTML][HTML] α-Aminoazoles/azines: key reaction partners for multicomponent reactions
S Imtiaz, S Banoo - RSC advances, 2021 - pubs.rsc.org
Aromatic α-aminoazaheterocycles are the focus of significant investigations and exploration
by researchers owing to their key role in diverse biological and physiological processes. The …
by researchers owing to their key role in diverse biological and physiological processes. The …
Contemporary progress in the synthetic strategies of imidazole and its biological activities
Heterocyclic compounds are pervasive in many areas of life and one of the heterocycles,
imidazole is a unique heterocyclic five-membered aromatic compound having two sp2 …
imidazole is a unique heterocyclic five-membered aromatic compound having two sp2 …
Diverse synthesis of pyrimido [1, 2-a] benzimidazoles and imidazo [2, 1-b] benzothiazoles via CuI-catalyzed decarboxylic multicomponent reactions of heterocyclic …
J Wu, H Luo, T Wang, H Sun, Q Zhang, Y Chai - Tetrahedron, 2019 - Elsevier
We have developed a straightforward approach to diverse synthesis of 2, 3-, 2, 4-
disubstituted pyrimido [1, 2-a] benzimidazoles, 2, 4, 10-trisubstituted 2, 10-dihydropyrimido …
disubstituted pyrimido [1, 2-a] benzimidazoles, 2, 4, 10-trisubstituted 2, 10-dihydropyrimido …
I 2/DMSO mediated multicomponent reaction for the synthesis of 2-arylbenzo [d] imidazo [2, 1-b] thiazole derivatives
Synthesis of a series of 2-arylbenzo [d] imidazo [2, 1-b] thiazoles tethered with barbituric acid
moiety has been reported from the three component reaction of 2-aminobenzothiazoles …
moiety has been reported from the three component reaction of 2-aminobenzothiazoles …
A new fluorescent probe based on imidazole [2, 1-b] benzothiazole for sensitive and selective detection of Cu2+
H Wang, S Zhao, Y Xu, L Li, B Li, M Pei… - Journal of Molecular …, 2020 - Elsevier
A simple fluorescent chemosensor WS1 (N'-[(Z)-1H-indazol-3-ylmethylidene] imidazo [2, 1-
b][1, 3] benzothiazole-2-carbohydrazide) based on imidazole [2, 1-b] benzothiazole was …
b][1, 3] benzothiazole-2-carbohydrazide) based on imidazole [2, 1-b] benzothiazole was …
Organocatalytic Synthesis of gem‐Difluorinated C2‐Spiro Indolines and Pyrimido[1,2‐a]benzimidazoles from 2‐Alkynyl‐3,3‐Difluoro‐3H‐Indoles
XY Mao, XT Lin, M Yang, GS Chen… - Advanced Synthesis & …, 2018 - Wiley Online Library
In this communication, we report a substrate‐controlled product diversity in the 1, 5, 7‐
triazabicyclo [4.4. 0] dec‐5‐ene (TBD)‐catalyzed cascade cyclization of 2‐alkynyl‐3, 3 …
triazabicyclo [4.4. 0] dec‐5‐ene (TBD)‐catalyzed cascade cyclization of 2‐alkynyl‐3, 3 …