1.8 Synthesis of (Trifluoromethyl)sulfanyl (SCF3) Compounds DOI
Chunfa Xu, Xinxin Shao,

Q. Shen

и другие.

Опубликована: Янв. 1, 2024

Abstract (Trifluoromethyl)sulfanyl compounds have garnered significant attention in medicinal chemistry, agrochemistry, and materials science due to their unique physicochemical properties, including high lipophilicity, metabolic stability, strong electron-withdrawing ability. This review pro-vides a comprehensive overview of the current methods for synthesis (trifluoromethyl)sulfanyl compounds, highlighting recent advances emerging strategies. Key synthetic approaches, such as direct (trifluoromethyl)sulfanylation, transition-metal-catalyzed processes, radical-based are discussed with an emphasis on substrates reagents. The chapter also briefly introduces mechanistic insights role novel reagents enhancing efficiency selectivity these transformations.

Язык: Английский

Copper‐Catalyzed Cyanoalkylation and Trifluoromethylthiolation of Styrene Derivatives via a Visible‐Light‐Promoted Cross‐Coupling DOI

Xiao‐Jing Xu,

Zhuomin Chi,

Rong Rui

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(11), С. 2607 - 2612

Опубликована: Март 26, 2024

Abstract Transition‐metal catalyzed difunctionalization of olefins has attracted considerable attention as a method to construct carbon‐carbon and carbon‐hetero bonds. Herein, the copper‐catalyzed three‐component radical cross‐coupling oxime esters, styrenes AgSCF 3 through visible‐light‐promoted iminyl radical‐mediated bond cleavage strategy been described. Utilizing low‐cost copper salt both photosensitizers cross‐couplers, this protocol delivers diverse target products, providing supplementary approach for cyanoalkylation trifluoromethylthiolation drug molecules.

Язык: Английский

Процитировано

2

Nickel-catalyzed regiodivergent sulfonylarylation of 1,3-enynes to access allenes and dienes DOI Creative Commons

Zhuomin Chi,

Yongchao Zhou,

Bingbing Liu

и другие.

Chemical Science, Год журнала: 2024, Номер 15(33), С. 13271 - 13278

Опубликована: Янв. 1, 2024

The radical-mediated difunctionalization of 1,3-enynes facilitates rapid access to structurally diverse allenes and dienes.

Язык: Английский

Процитировано

1

Palladium-catalyzed four-component domino sulfonylation and carbonylation of 1,3-enynes at room temperature DOI
Jing Wang, Jun Ying

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(20), С. 5851 - 5858

Опубликована: Янв. 1, 2024

A novel palladium-catalyzed four-component domino sulfonylation and carbonylation of 1,3-enynes has been developed, which enables the rapid incorporation allene, sulfone, carbonyl amine units into one single molecule simultaneously.

Язык: Английский

Процитировано

1

The Road to Green Efficiency: Exploration of multicomponent reactions from transition metal catalysis to no catalyst conditions DOI
Jie Li, Jiabin Cui,

Hongying Guo

и другие.

Reaction Chemistry & Engineering, Год журнала: 2024, Номер 10(3), С. 500 - 510

Опубликована: Дек. 20, 2024

Multicomponent reactions (MCRs) have become excellent tools for synthesizing complex and high-value molecules. This minireview highlights recent progresses in MCRs classified by the type of catalysts to offer a better deeper understanding.

Язык: Английский

Процитировано

1

Copper-catalyzed sulfonamidation of enol silyl ether via SO2 insertion towards the synthesis of β-keto sulfonamides DOI

Qinqiong Zeng,

Yujia Gong,

Xuemei Zhang

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(13), С. 3589 - 3595

Опубликована: Янв. 1, 2024

This method offers a simple, effective pathway for synthesizing diverse β-keto sulfonamides with satisfactory yields under mild conditions, showing broad substrate compatibility and good tolerance towards various functional groups.

Язык: Английский

Процитировано

0

Brønsted base catalyzed Reppe sulfonylation reaction DOI
X. He, Xiaohong Wang, Fei Zhou

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(17), С. 4740 - 4747

Опубликована: Янв. 1, 2024

The Reppe sulfonylation reaction has remained substantially underexplored. We present a novel method for involving SO 2 insertion, remarkably without the need metal catalysts, instead utilizing Brønsted bases as catalysts.

Язык: Английский

Процитировано

0

1.8 Synthesis of (Trifluoromethyl)sulfanyl (SCF3) Compounds DOI
Chunfa Xu, Xinxin Shao,

Q. Shen

и другие.

Опубликована: Янв. 1, 2024

Abstract (Trifluoromethyl)sulfanyl compounds have garnered significant attention in medicinal chemistry, agrochemistry, and materials science due to their unique physicochemical properties, including high lipophilicity, metabolic stability, strong electron-withdrawing ability. This review pro-vides a comprehensive overview of the current methods for synthesis (trifluoromethyl)sulfanyl compounds, highlighting recent advances emerging strategies. Key synthetic approaches, such as direct (trifluoromethyl)sulfanylation, transition-metal-catalyzed processes, radical-based are discussed with an emphasis on substrates reagents. The chapter also briefly introduces mechanistic insights role novel reagents enhancing efficiency selectivity these transformations.

Язык: Английский

Процитировано

0