Photocatalytic Ring-Closing Metathesis/Amination of 1,6-Enynes and 1,7-Enynes: Synthesis of α,β-Unsaturated γ-Lactams and Quinolin-2-ones DOI
Juan Ren, Tian‐Yu Sun, Xiao‐Feng Xia

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Май 20, 2025

A photocatalyzed ring-closing metathesis/amination of 1,6-enynes and 1,7-enynes using alkyl oxime esters as both an alkene deconstruction auxiliary amination source is present for the synthesis α,β-unsaturated γ-lactams quinolin-2-ones. Preliminary mechanistic studies suggest that intramolecular 1,5-hydrogen atom transfer key to generation unstabilized radicals, which subsequently promote homolytic Cα-Cβ cleavage under driving force formation more stable captodative radicals.

Язык: Английский

g-C3N4-Based Heterogeneous Photocatalyzed Synthesis and Evaluation of Antitumor Activities of Fluoroalkylated 4H-Pyrido[1,2-a]pyrimidin-4-ones DOI
Ningbo Li, Yan Liu,

Chu-Qian Hu

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Фев. 26, 2025

The first example of heterogeneous photoredox-catalyzed fluoroalkylation 4H-pyrido[1,2-a]pyrimidin-4-ones has been developed. With low-cost commercial g-C3N4 as the recyclable photocatalyst and cheap sodium fluoroalkyl sulfonates source, a variety fluoroalkylated pyridopyrimidinones were constructed in moderate to high yields. present reaction can be easily scaled up with good efficiency, catalytic system reused 5 times slight loss activities. Furthermore, biological activity synthesized compounds was preliminarily investigated.

Язык: Английский

Процитировано

0

Photocatalytic Ring-Closing Metathesis/Amination of 1,6-Enynes and 1,7-Enynes: Synthesis of α,β-Unsaturated γ-Lactams and Quinolin-2-ones DOI
Juan Ren, Tian‐Yu Sun, Xiao‐Feng Xia

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Май 20, 2025

A photocatalyzed ring-closing metathesis/amination of 1,6-enynes and 1,7-enynes using alkyl oxime esters as both an alkene deconstruction auxiliary amination source is present for the synthesis α,β-unsaturated γ-lactams quinolin-2-ones. Preliminary mechanistic studies suggest that intramolecular 1,5-hydrogen atom transfer key to generation unstabilized radicals, which subsequently promote homolytic Cα-Cβ cleavage under driving force formation more stable captodative radicals.

Язык: Английский

Процитировано

0