Paper
TBAB-mediated radical 6-endo-trig ortho-cyclization of N-aryl-N-(prop-2-yn-1-yl)benzenesulfonamide for the synthesis of 3-bromo-1,2-dihydroquinoline
Published Jun 21, 2019 · Min Yang, Xin Hu, Banlai Ouyang
Tetrahedron
Q3 SJR score
6
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
This study presents a new synthetic route for 3-bromo-1,2-dihydroquinoline derivatives using TBAB/Oxone-mediated radical 6-endo-trig ortho-cyclization of 2-alkynylbenzamide, with high reaction efficiency and moderate functional group tolerance.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Sign up to use Study Snapshot
Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.
Full text analysis coming soon...
References
Synthesis of 3-(Bromomethylene)isobenzofuran-1(3H)-ones through regioselective 5-exo-dig bromocyclization of 2-alkynylbenzoic acids
This study developed a regioselective 5-exo-dig bromocyclization method for the direct synthesis of 3-(bromomethylene)isobenzofuran-1(3H)-ones from 2-alkynylbenzoic acids, with potential applications in heterocycle conversion
2019·34citations·Yan‐Long Zheng et al.·Tetrahedron
Tetrahedron
Synthesis of β-Sulfonyl Amides through a Multicomponent Reaction with the Insertion of Sulfur Dioxide under Visible Light Irradiation.
This study demonstrates an efficient and selective synthesis of -sulfonyl amides from styrenes using a multicomponent reaction with sulfur dioxide under visible light irradiation.
2019·67citations·Yu Zong et al.·Organic letters
Organic letters
AgBF4-catalyzed deoxygenative C2-amination of quinoline N-oxides with isothiocyanates
This study developed a general, effective, and convenient protocol for the direct synthesis of various 2-aminoquinolines under base-, oxidant-free, and mild conditions.
2019·54citations·Long-Yong Xie et al.·Organic Chemistry Frontiers
Organic Chemistry Frontiers
Natural Deep Eutectic Solvent-Catalyzed Selenocyanation of Activated Alkynes via an Intermolecular H-Bonding Activation Process
Natural deep eutectic solvents can efficiently catalyze selective selenocyanation of activated alkynes, enabling efficient construction of various Z-vinyl selenolates.
2019·102citations·Chao Wu et al.·ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering
Metal-free difunctionalization of alkynes leading to alkenyl dithiocyanates and alkenyl diselenocyanates at room temperature.
This study developed a simple, metal-free method for synthesis of alkenyl dithiocyanates and alkenyl diselenocyanates at room temperature, using oxone and PhI(OAc)2 as oxidants.
2018·58citations·Ling-Hui Lu et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry
Multicatalytic Beckmann rearrangement of 2-hydroxylarylketone oxime: Switchable synthesis of benzo[d]oxazoles and N-(2-hydroxylaryl)amides
This study developed a switchable synthesis route for benzo[d]oxazole derivatives and (2-hydroxylaryl)benzamide from 2-hydroxylbenzeneketoxime using organomolecules and Lewis acid cocatalyzed Beckmann rearrangement.
2018·10citations·Zhen Li et al.·Tetrahedron Letters
Tetrahedron Letters
Metal-free deoxygenative sulfonylation of quinoline N-oxides with sodium sulfinates via a dual radical coupling process
This study presents a metal- and reductant-free deoxygenative sulfonylation of quinoline N-oxides with sodium sulfinates, a novel method that complements current methods for radical reaction of quinoline N-oxides.
2018·95citations·Long-Yong Xie et al.·Organic chemistry frontiers
Organic chemistry frontiers
Ultrasound-promoted Brønsted acid ionic liquid-catalyzed hydrothiocyanation of activated alkynes under minimal solvent conditions
Ultrasound-promoted Bronsted acid ionic liquid-catalyzed hydrothiocyanation of activated alkynes under minimal solvent conditions provides an eco-friendly, practical, and efficient method for synthesis of Z-vinyl thiocyanates.
2018·148citations·Chao Wu et al.·Green Chemistry
Green Chemistry
Citations
Electrochemical C-H Mono-/Multi-Bromination Regulation of N-Sulfonylanilines on a Cost-Effective Carbon Fiber Electrode and Its Prospective Electroactive Molecule Screening.
Electrochemical C-H mono/multi-bromination of N-sulfonylanilines on a cost-effective carbon fiber electrode produces diverse mono/multi-brominated anilines with potential applications in electrochemical biosensors.
2024·0citations·Shuchun Xie et al.·The Journal of organic chemistry
The Journal of organic chemistry
Photocatalytic Cyclization Cascades by Radical Relay toward Pyrrolo[1,2-a]indoles: Synthesis, Mechanism, and Application.
Photocatalytic cyclization cascades using radical relay and hydrogen-atom-abstraction processes can produce tri/difluoromethylated pyrrolo[1,2-a]indoles, useful for fluorescent dyes and live-cell imaging.
2024·6citations·Chen He et al.·The Journal of organic chemistry
The Journal of organic chemistry
Recent Advances in the Oxone-Mediated Synthesis of Heterocyclic Compounds
Oxone-mediated synthesis has advanced to produce diverse N-, O-, and chalcogen-containing heterocyclic compounds, with advantages, scope, and limitations.
2021·8citations·Helen A. Goulart et al.·Molecules
Molecules
Recent Advances in Transition Metal Free Synthetic Protocols for Quinoline Derivatives
Transition metal-free synthetic routes have developed to produce a wide variety of substituted quinolines with potential therapeutic activities.
2020·3citations·R. Tabassum et al.·Current Organic Chemistry
Current Organic Chemistry
ZnBr2/Oxone-mediated ipso-cyclization of N-(3-phenylprop-2-yn-1-yl)aniline
This study developed a selective synthetic strategy towards 1-azaspiro[4.5]deca-3,6,9-trien-8-ones from N-tosyl-N-(prop-2-yn-1-yl)aniline using ZnBr2 and Oxone in a mixed solvent, demonstrating
2019·4citations·Keke Huang et al.·RSC Advances
RSC Advances