Pd-catalyzed imine-directed one-pot access to polysubstituted pyrroles via tandem triple isocyanide insertion/aza-Nazarov cyclization reactions
J Li, ZW Zhao, S Zheng, P He, JY Qiu… - Organic Chemistry …, 2023 - pubs.rsc.org
Herein, we report a novel one-pot method for synthesizing polysubstituted pyrrole
derivatives via three-component reactions of alkenyl bromides, amines, and isocyanides …
derivatives via three-component reactions of alkenyl bromides, amines, and isocyanides …
Solvent-free Approaches towards the Synthesis of Therapeutically Important Heterocycles
A Priyadarshan, G Tripathi, AK Singh… - Current Green …, 2024 - ingentaconnect.com
The development of synthetic methodologies to obtain a diverse range of heterocyclic
scaffolds has been a very attractive area of research due to their vast therapeutic …
scaffolds has been a very attractive area of research due to their vast therapeutic …
Solvent-free and ball mill-free catalytic C–H methylation
M Hribersek, C Méndez-Gálvez, M Huber, PJ Gates… - Green …, 2023 - pubs.rsc.org
An expedient, mechanochemical, operationally simple protocol is reported for the Rh-
catalysed C–H methylation of (hetero) arenes under solvent-free conditions without the use …
catalysed C–H methylation of (hetero) arenes under solvent-free conditions without the use …
Divergent Conversion of Double Isocyanides with Alkenyl Bromide to Polysubstituted Pyrroles and 4-Imino-4,5-dihydropyrrolo[3,4-b]pyrrol-6(1H)-one Derivatives by …
ZL Ren, JY Qiu, LL Yuan, YF Yuan, S Cai, J Li… - Organic …, 2022 - ACS Publications
Herein a novel and concise approach to pyrrole skeletons via Pd-catalyzed tandem
cyclization reactions is investigated. The substrates for the transformation could be readily …
cyclization reactions is investigated. The substrates for the transformation could be readily …
Visible-Light-Induced Oxyalkylation of 1,2,4-Triazine-3,5(2H, 4H)-diones with Ethers via Oxidative Cross-Dehydrogenative Coupling
Y Tan, W Xuekun, YP Han, Y Zhang… - The Journal of …, 2022 - ACS Publications
An efficient and convenient method to synthesize 6-oxyalkylated 1, 2, 4-triazine-3, 5 (2 H, 4
H)-diones has been developed via visible-light-induced cross-dehydrogenative coupling …
H)-diones has been developed via visible-light-induced cross-dehydrogenative coupling …
Visible light-induced synthesis of biomass-derived quinoxaline by using Co phthalocyanine immobilized on pyridine-doped g-C3N4
M Jin, SM Sadeghzadeh, J Chen - Journal of Energy Chemistry, 2023 - Elsevier
Visible light-driven valorization of biomass has recently been a pioneering field for nitrogen-
containing heterocyclics syntheses due to its sustainable features. Herein, various aromatic …
containing heterocyclics syntheses due to its sustainable features. Herein, various aromatic …
Recent Advances in Selective CH Bonds Functionalization through Aryl Radical Mediated Hydrogen Atom Transfer Strategy
L Xing, Y Zhang - Current Organic Chemistry, 2023 - ingentaconnect.com
Selective CH bond functionalization of organic molecules has developed as an increasingly
versatile platform that found wide applications in the synthesis of naturally occurring …
versatile platform that found wide applications in the synthesis of naturally occurring …
B(C6F5)3-Catalyzed Multicomponent Reactions of 2,3-Diketoesters, Amines, Allenes, and Nucleophiles: Synthesis of 2α-Functionalized Pyrroles
WW Zhang, Q Sha - The Journal of Organic Chemistry, 2024 - ACS Publications
An efficient B (C6F5) 3-catalyzed multicomponent reaction of 2, 3-diketoesters, amines,
allenes, and nucleophiles was reported, which afforded 2α-functionalized pyrroles in …
allenes, and nucleophiles was reported, which afforded 2α-functionalized pyrroles in …
Facile synthesis of 5α-functionalized pyrroles via multicomponent reactions of vicinal tricarbonyl compounds, enamines, and nucleophiles
H Wan, Z Shi, Q Sha - Organic Chemistry Frontiers, 2024 - pubs.rsc.org
Pyrrole is a versatile heterocyclic moiety that is widely used in many areas, while methods
for the direct synthesis of α-functionalized pyrroles are still limited. We report herein novel B …
for the direct synthesis of α-functionalized pyrroles are still limited. We report herein novel B …
One-pot domino synthesis of 1, 2, 4-triazolo [3, 4-b][1, 3, 4] 6-amino thiadiazines and their CT-DNA binding study
A facile one-pot three component domino protocol has been successfully developed for the
combinatorial synthesis of novel Schiff bases of 3-(2-(6-amino-7H-[1, 2, 4]-triazolo [3, 4-b][1 …
combinatorial synthesis of novel Schiff bases of 3-(2-(6-amino-7H-[1, 2, 4]-triazolo [3, 4-b][1 …