Chinese Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 43(11), P. 3679 - 3679
Published: Jan. 1, 2023
Language: Английский
Chinese Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 43(11), P. 3679 - 3679
Published: Jan. 1, 2023
Language: Английский
Asian Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 13(5)
Published: Feb. 16, 2024
Abstract Fused quinolines have gained substantial attention due to their significant biological and wide‐spectrum synthetic applications. This review supplies an encyclopedic document regarding the approaches developed for synthesis of fused‐cyclic based on ring volume size reported thus far. collected information will be valuable medicinal chemists obtain knowledge designing new in order access active compounds.
Language: Английский
Citations
6Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(30)
Published: May 23, 2023
Abstract A rhodium(III)‐catalyzed oxidative cyclization of chalcones with internal alkynes is reported, generating biologically important 3,3‐disubstituted 1‐indanones along reusable aromatic aldehydes. This transformation features unique (4+1) reaction mode, excellent regioselectivity in alkyne insertion, broad substrate scope, allows for the construction quaternary carbon centers, and scalable. Steric hindrance from ligand probably controls chemoselectivity this carbocyclization. Importantly, discovery enables a practical two‐step protocol switching overall acetophenones (3+2) to annulation.
Language: Английский
Citations
9Organic Chemistry Frontiers, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
The synthesis of benzofuranone-based spiropyrans containing a thiophene, benzothiophene, or indole moiety, their diverse temperature-dependent photochromic properties, and DFT rationalization.
Language: Английский
Citations
0Molecules, Journal Year: 2023, Volume and Issue: 28(12), P. 4725 - 4725
Published: June 12, 2023
Sequential reactions of aminoalkynes represent a powerful tool to easily assembly biologically important polyfunctionalized nitrogen heterocyclic scaffolds. Metal catalysis often plays key role in terms selectivity, efficiency, atom economy, and green chemistry these sequential approaches. This review examines the existing literature on applications with carbonyls, which are emerging for their synthetic potential. Aspects concerning features starting reagents, catalytic systems, alternative reaction conditions, pathways possible intermediates provided.
Language: Английский
Citations
5Published: May 17, 2023
Sequential reactions of aminoalkynes represent a powerful tool to easily assembly biologically important polyfunctionalized nitrogen heterocyclic scaffolds. Metal catalysis often plays key role in terms selectivity, efficiency, atom economy and green chemistry these sequential approaches. This review examines the existing literature on applications with carbonyls which are emerging for their synthetic potential. Aspect concerning features starting reagents, catalytic systems, alternative reaction conditions pathways as well possible intermediates provided.
Language: Английский
Citations
4Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(10), P. 1079 - 1083
Published: Jan. 23, 2024
Comprehensive Summary A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products used as a versatile linchpin for synthesis structurally diverse functional dibenzoullazines that are difficult to access other synthetic methods.
Language: Английский
Citations
1Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: 366(10), P. 2312 - 2323
Published: March 28, 2024
Abstract A range of densely functionalized ullazines have been synthesized by a one‐pot Rh(III)‐catalyzed twofold C−H activation/oxidative annulation N ‐arylpyrroles with alkynes. Electrophilic bromination at 5‐ or 5,7‐ positions the EWG‐substituted ullazine core offers an interesting single double entry for further extended functionalization. Mechanistic considerations suggest two complementary paths, EWG‐assisted and S E Ar, activations. All exhibit strong fluorescence emissions. Ullazines bearing thiophene triarylamine units show significant bathochromic shift in their emission spectra, attributed to more electronic circuits present.
Language: Английский
Citations
1Chemical Science, Journal Year: 2023, Volume and Issue: 14(40), P. 11203 - 11212
Published: Jan. 1, 2023
An aza-dicyclopenta[ a , g ]naphthalene scaffold was discovered as controllable luminogenic structure, and precise balance of molecular motions unlocks the remarkable narrowband AIEgens.
Language: Английский
Citations
1Tetrahedron, Journal Year: 2024, Volume and Issue: 166, P. 134224 - 134224
Published: Aug. 30, 2024
Language: Английский
Citations
0Angewandte Chemie, Journal Year: 2023, Volume and Issue: 135(30)
Published: May 23, 2023
Abstract A rhodium(III)‐catalyzed oxidative cyclization of chalcones with internal alkynes is reported, generating biologically important 3,3‐disubstituted 1‐indanones along reusable aromatic aldehydes. This transformation features unique (4+1) reaction mode, excellent regioselectivity in alkyne insertion, broad substrate scope, allows for the construction quaternary carbon centers, and scalable. Steric hindrance from ligand probably controls chemoselectivity this carbocyclization. Importantly, discovery enables a practical two‐step protocol switching overall acetophenones (3+2) to annulation.
Language: Английский
Citations
0