Chem Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 101159 - 101159
Published: Nov. 1, 2024
Language: Английский
Chem Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 101159 - 101159
Published: Nov. 1, 2024
Language: Английский
Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(34), P. 6988 - 6998
Published: Jan. 1, 2024
Herein, an N-heterocyclic carbene (NHC) catalyzed radical tandem cyclization reaction of
Language: Английский
Citations
1Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 10, 2024
Comprehensive Summary A visible‐light‐induced decarboxylative radical cascade cyclization reaction between N ‐(2‐cyanoaryl)‐acrylamides and alkyl ‐(acyloxy)phthalimide (NHPI esters) for the construction of phenanthridine derivatives has been developed. This approach utilizes lithium iodide (LiI) triphenylphosphine (PPh 3 ) as redox catalysts is produced through photoactivation electron donor‐acceptor (EDA) complex. series primary, secondary, tertiary alkyl‐substituted phenanthridines are prepared in up to 82% yield without transition‐metal catalysts, chemical oxidants, or metal‐/organic dye‐based photocatalysts.
Language: Английский
Citations
1Synlett, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 4, 2024
Abstract A mild, metal, and photoredox-free direct arylation of alkyl aryl thiols with iodides using a DMF/KOt-Bu system has been developed. In the absence an N-heterocyclic carbene (NHC) additive, reaction proceeds via benzyne intermediate was suitable for substitution phenyl, while presence NHC or phenanthroline derivative improves regioselectivity substituted radical pathway. This protocol features inexpensive materials good substrate scope could be useful in thiols.
Language: Английский
Citations
0Chem Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 101159 - 101159
Published: Nov. 1, 2024
Language: Английский
Citations
0