Copper-catalyzed regio- and chemoselective selenosulfonylation of 1,6-enynes from sulfur dioxide DOI
Fu‐Sheng He,

Yanfang Yao,

Zhimei Tang

и другие.

Organic Chemistry Frontiers, Год журнала: 2021, Номер 8(21), С. 6119 - 6124

Опубликована: Янв. 1, 2021

An efficient copper-catalyzed multicomponent reaction of 1,6-enynes, diselenides, DABCO·(SO 2 ) , and cycloketone oxime esters was achieved, providing cyanoalkylsulfonated pyrrolidines in moderate to good yields.

Язык: Английский

Advances in Oxosulfonylation Reaction DOI
Sumit Ghosh, Sadhanendu Samanta, Asim Kumar Ghosh

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2020, Номер 362(21), С. 4552 - 4578

Опубликована: Авг. 21, 2020

Abstract Oxosulfonylation is a difunctionalization protocol where oxo and sulfonyl groups are introduced in one step to construct ketosulfones N ‐acylsulfonamides from simple readily accessible reagents. The development of oxosulfonylation methods has gained significant attention due their importance organic medicinal chemistry. This review article provides brief concise overview the current status latest methodologies using green oxidant sources for reactions developed last two decades. magnified image

Язык: Английский

Процитировано

40

A visible-light photoredox-catalyzed four-component reaction for the construction of sulfone-containing quinoxalin-2(1H)-ones DOI

Yufen Lv,

Jinyun Luo,

Muze Lin

и другие.

Organic Chemistry Frontiers, Год журнала: 2021, Номер 8(19), С. 5403 - 5409

Опубликована: Янв. 1, 2021

A visible-light photoredox-catalyzed four component reaction of quinoxalin-2(1 H )-ones, alkenes, aryldiazonium, and sodium metabisulfite leading to sulfone-containing )-ones has been developed.

Язык: Английский

Процитировано

39

Metal‐Free Visible‐light Mediated C−S Bond Formation DOI
Ashish Kumar Sahoo,

Dinabandhu Barik,

Binoyargha Dam

и другие.

Asian Journal of Organic Chemistry, Год журнала: 2023, Номер 12(8)

Опубликована: Июнь 26, 2023

Abstract The upsurge in interest the development of methodologies for synthesis sulfur‐containing compounds via use visible‐light has been established as a sustainable tool organic chemistry. Particularly, mediated C−S bond formation gained popularity due to its operational simplicity, minimized by‐products, easy handling, mild reaction conditions, etc. Photochemistry not only provides way synthesize complex molecules but also ability overcome many challenges which are difficult attain by conventional thermal pathways. Owing biological importance compounds, present review focused on under metal‐free conditions visible‐light. objective current is bring out unearthing collection regarding photoredox catalysis. For better understanding, categorized according mode reactions viz , difunctionalization alkenes and alkynes, C−H functionalization, radical cyclization. All each sections described with selected examples proper explanation proposed mechanism.

Язык: Английский

Процитировано

16

Heterogeneous Photocatalytic C–H Functionalization of Indoles with Diazo Compounds Enabled by Carbon Nitride DOI
Peiying Li, Rong Chang,

Fujun Guan

и другие.

The Journal of Organic Chemistry, Год журнала: 2023, Номер 88(13), С. 8703 - 8708

Опубликована: Май 29, 2023

Herein, we reported the heterogeneous photocatalytic C–H alkylation of indoles with diazo compounds using graphitic carbon nitride (g-C3N4) as photocatalyst. The reaction was carried out under a simple operation and mild conditions. In addition, catalyst found to be stable reusable after five cycles. photochemical proceeds via an intermediary radical, which is generated from through visible-light-promoted proton-coupled electron transfer (PCET) process.

Язык: Английский

Процитировано

14

Copper-catalyzed regio- and chemoselective selenosulfonylation of 1,6-enynes from sulfur dioxide DOI
Fu‐Sheng He,

Yanfang Yao,

Zhimei Tang

и другие.

Organic Chemistry Frontiers, Год журнала: 2021, Номер 8(21), С. 6119 - 6124

Опубликована: Янв. 1, 2021

An efficient copper-catalyzed multicomponent reaction of 1,6-enynes, diselenides, DABCO·(SO 2 ) , and cycloketone oxime esters was achieved, providing cyanoalkylsulfonated pyrrolidines in moderate to good yields.

Язык: Английский

Процитировано

31