Strategic Synthesis of Sulfinamides as Versatile S(IV) Intermediates DOI Creative Commons
Subham Das,

Amit Dhibar,

Basudev Sahoo

и другие.

ACS Organic & Inorganic Au, Год журнала: 2024, Номер 5(1), С. 1 - 12

Опубликована: Ноя. 30, 2024

Sulfinamides constitute adaptable S(IV) intermediates with a sulfur stereocenter, having emerging interest in divergent synthesis of high-valent S(VI) functional bioisosteres. Recent years have witnessed the strategic development mild and selective synthetic routes for highly functionalized sulfinamides, employing stable organometallic reagents, carbon-centered radical precursors, other abundant coupling partners merged various reagents arena metal, photoredox, organocatalysis. Furthermore, asymmetric metal organocatalysis enabled stereoselective enantioenriched sulfinamides. In this Perspective, we present recent (2021 to present) advancement methods toward

Язык: Английский

Visible-light induced direct C(sp3)–H functionalization: recent advances and future prospects DOI
Jia‐Lin Tu, Yining Zhu, Pengcheng Li

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(18), С. 5278 - 5305

Опубликована: Янв. 1, 2024

This review summarizes the latest methodological advances in photocatalytic C(sp 3 )–H functionalization, with a particular emphasis on formation of C–P, C–B, C–S bonds, etc ., and some prominent efforts asymmetric C–H functionalization.

Язык: Английский

Процитировано

15

The Catalytic Synthesis of Aza-Sulfur Functional Groups DOI
Michael C. Willis,

Ming-Kai Wei

Synthesis, Год журнала: 2024, Номер unknown

Опубликована: Сен. 26, 2024

Abstract Sulfur-containing compounds are found in myriad applications. Sulfones and sulfonamides the most common functional groups used medicinal agrochemical endeavours. Isosteres of these groups, for example, sulfoximines sulfonimidamides, emerging functionalities, they increasingly relevant patent literature. However, general, associated synthetic routes still have limitations, including use harsh reaction conditions highly reactive reagents. A variety catalytic reactions that employ a diverse range substrate classes been developed to address issues. This short review highlights recent syntheses aza-sulfur compounds, which we hope will open new directions discovery chemistry. 1 Introduction 2 Reactions N-Sulfinylamines 3 with Sulfenamides 4 Sulfinates 5 Sulfinamides 6 Other Aza-Sulfur Compounds 7 Conclusion

Язык: Английский

Процитировано

4

Iron Photoredox Catalysis as an Effective Tool for Organic Synthesis via Visible‐Light‐Induced Homolysis (VLIH) DOI
Vishal Srivastava, Praveen P. Singh, Surabhi Sinha

и другие.

ChemistrySelect, Год журнала: 2025, Номер 10(4)

Опубликована: Янв. 1, 2025

Abstract Owing to its possible advantages for the environment and economy, photoredox catalysis of organic processes fueled by iron has garnered a lot interest recently. The potential photo‐induced single‐electron transfer (SET) events occurring outside sphere is now well acknowledged. Currently, focus shifted newly discovered photoactivation method that based on an inner‐sphere mode reactivity caused population visible‐light‐induced homolysis (VLIH) states. VLIH activation, in contrast photoredox, specific complexes, offers distinct profiles, does not require redox potentials coincide. These attractive properties have prompted development strategies use this blueprint manufacture highly reactive open‐shell species mild environments. purpose contribution promote novel synthetic techniques sustainable chemical transformations offer educational instrument understanding evolving idea.

Язык: Английский

Процитировано

0

Photoredox-catalyzed deoxygenative radical transformation of alcohols to sulfinamides DOI Creative Commons
Xinyu Zhu, Junliang Wu, Junliang Zhang

и другие.

RSC Advances, Год журнала: 2025, Номер 15(6), С. 4532 - 4535

Опубликована: Янв. 1, 2025

Sulfinamides play a crucial role in organic synthesis and pharmaceuticals.

Язык: Английский

Процитировано

0

Synthesis of amides via TBN-induced oxidation cross-coupling of acetonitrile and N -sulfinylanilines DOI

Quansen Wu,

Zhuang Ma, Rui Li

и другие.

Synthetic Communications, Год журнала: 2025, Номер unknown, С. 1 - 9

Опубликована: Апрель 21, 2025

Язык: Английский

Процитировано

0

Photochemical upcycling of polymers via visible light-driven C−H bond activation DOI
Yi Wei, Jing Liu, Xiao‐Qiang Hu

и другие.

Chemical Communications, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

This mini-review highlights the scientific breakthroughs in photochemical upcycling polymers through oxidative degradation and post-polymerization modification via visible light-driven C–H bond activation.

Язык: Английский

Процитировано

3

Photocatalyst-Free Transformation of C(sp3)–H Bonds to Oxime Ethers via Photoinduced Hydrogen Atom Transfer DOI

Yulian Zhao,

Xuehong Min,

Lijing Li

и другие.

Organic Letters, Год журнала: 2024, Номер 26(43), С. 9383 - 9388

Опубликована: Окт. 22, 2024

Herein, a direct transformation of aliphatic C–H bonds to oxime ethers has been developed via light-promoted hydrogen atom transfer (HAT) in the absence photocatalyst. Singlet oxygen and chlorine radical are complementary C(sp3)–H bond cleaving agents this reaction, enabling extraction atoms from diverse range compounds, like cycloalkanes, ethers, amines, amides, cyclic sulfides. This method excels transforming common into valuable featuring abundant chemical feedstocks, good functional group tolerance, catalyst free conditions.

Язык: Английский

Процитировано

0

Strategic Synthesis of Sulfinamides as Versatile S(IV) Intermediates DOI Creative Commons
Subham Das,

Amit Dhibar,

Basudev Sahoo

и другие.

ACS Organic & Inorganic Au, Год журнала: 2024, Номер 5(1), С. 1 - 12

Опубликована: Ноя. 30, 2024

Sulfinamides constitute adaptable S(IV) intermediates with a sulfur stereocenter, having emerging interest in divergent synthesis of high-valent S(VI) functional bioisosteres. Recent years have witnessed the strategic development mild and selective synthetic routes for highly functionalized sulfinamides, employing stable organometallic reagents, carbon-centered radical precursors, other abundant coupling partners merged various reagents arena metal, photoredox, organocatalysis. Furthermore, asymmetric metal organocatalysis enabled stereoselective enantioenriched sulfinamides. In this Perspective, we present recent (2021 to present) advancement methods toward

Язык: Английский

Процитировано

0