Journal of Solid State Chemistry, Journal Year: 2024, Volume and Issue: 340, P. 125006 - 125006
Published: Sept. 10, 2024
Language: Английский
Journal of Solid State Chemistry, Journal Year: 2024, Volume and Issue: 340, P. 125006 - 125006
Published: Sept. 10, 2024
Language: Английский
Organic Chemistry Frontiers, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Herein, an environmentally friendly methodology has been established for the photoelectrochemical chlorination of C(sp 2 )–H bonds in quinolinone derivatives using PVC plastic waste as chlorine source.
Language: Английский
Citations
2Molecular Catalysis, Journal Year: 2024, Volume and Issue: 565, P. 114379 - 114379
Published: July 9, 2024
Language: Английский
Citations
5Chinese Journal of Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: April 17, 2025
Comprehensive Summary A practical photocatalytic annulation‐biselenylation strategy has been developed for the efficient synthesis of biselenium‐substituted 1‐indanones (38 examples in total) with generally good yields (up to 95%) and excellent stereoselectivity (>19 : 1 Z / E ratio) by employing enynones diaryl selenides as starting materials under photosensitizer‐free conditions. The reaction mechanism involves a cascade process comprising homolytic cleavage, radical addition, 5‐ exo ‐ dig cyclization, capture, enabling sequential formation multiple bonds, such C(sp 3 )‐Se, )‐C(sp 2 ), )‐Se rapidly construct molecular complexity. Notably, this approach demonstrates wide substrate compatibility tolerability towards various functional groups. It is further characterized its remarkable efficiency creating chemical bonds achieving high atomic utilization 100%.
Language: Английский
Citations
0Molecules, Journal Year: 2024, Volume and Issue: 29(20), P. 4815 - 4815
Published: Oct. 11, 2024
A biomass-based catalyst, CuxOy@CS-400, was employed as an excellent recyclable heterogeneous catalyst to realize the sulfonylation reaction of aniline derivatives with sodium sulfinates. Various substrates were compatible, giving desired products moderate good yields at room temperature. In addition, this copper also easy recover and up five times without considerably deteriorating in catalytic efficiency. Importantly, these readily converted corresponding 4-sulfonyl anilines via a hydrolysis step. The method offers unique strategy for synthesizing arylsulfones has potential create new possibilities developing copper-catalyzed C-H functionalizations.
Language: Английский
Citations
1Journal of Solid State Chemistry, Journal Year: 2024, Volume and Issue: 340, P. 125006 - 125006
Published: Sept. 10, 2024
Language: Английский
Citations
0