Iodine-Promoted Disproportionate Coupling Reaction of Arylsulfonyl Hydrazides: A Simple and Green Access to Thiosulfonates DOI
Qi Chen,

Zhao-Hua Chen,

Shi‐Wei Yu

и другие.

Synthesis, Год журнала: 2024, Номер 56(09), С. 1415 - 1421

Опубликована: Янв. 17, 2024

Abstract An environmentally friendly iodine-promoted disproportionate coupling reaction of arylsulfonyl hydrazides is reported. This strategy can synthesize thiosulfonates with medium to excellent yields, and features a green system, wide applicability substrates, easy availability raw materials. The preliminary mechanistic study reveals that iodine plays an important role in the radical process.

Язык: Английский

Construction of C−S and C−Se Bonds from Unstrained Ketone Precursors under Photoredox Catalysis DOI Creative Commons
Hao Wu, Shuguang Chen,

Chunni Liu

и другие.

Angewandte Chemie International Edition, Год журнала: 2024, Номер 63(8)

Опубликована: Янв. 8, 2024

A mild photoredox catalyzed construction of sulfides, disulfides, selenides, sulfoxides and sulfones from unstrained ketone precursors is introduced. Combination this deacylative process with S

Язык: Английский

Процитировано

23

Xylan derived fluorescence carbon dots composite with cotton cellulose paper as ‘turn-off’ fluorescence platform for sensitive and selective detection Cu2+ in real samples DOI
Yingying Zhang,

Xiuyuan Feng,

Zhiyuan Chen

и другие.

International Journal of Biological Macromolecules, Год журнала: 2023, Номер 254, С. 127707 - 127707

Опубликована: Ноя. 1, 2023

Язык: Английский

Процитировано

19

Cross-Electrophile Couplings of Benzyl Sulfonium Salts with Thiosulfonates via C–S Bond Activation DOI

Xuan-Bo Hu,

Yuwei Chen, Chenlong Zhu

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(18), С. 13601 - 13607

Опубликована: Сен. 4, 2024

A zinc-mediated cross-electrophile coupling of benzyl sulfonium salts with thiosulfonates via C-S bond cleavage was achieved. The reductive thiolation proceeded well under transition metal-free conditions to afford the desired sulfides in good yields, exhibiting both broad substrate scope and functionality tolerance. In addition, reaction could be applied use selenosulfonate as an effective selenylation agent subjected scale-up synthesis.

Язык: Английский

Процитировано

7

Divergent Trideuteromethylthiolation and Aminotrideuteromethylthiolation of Alkenes with N-Fluorobenzenesulfonimide and CD3SSO3Na DOI

Wenting Wang,

Lin Zhao,

Hui Wu

и другие.

Organic Letters, Год журнала: 2023, Номер 25(39), С. 7078 - 7082

Опубликована: Сен. 21, 2023

A metal-free oxidative trideuteromethylthiolation of alkenes with CD3SSO3Na using NFSI as an oxidant has been developed. The aminotrideuteromethylthiolation a three-component reaction could be easily achieved in the presence cobalt catalyst. divergent alkenes, readily available reagent, and versatile synthetic strategy allow for late-stage modification drug molecules.

Язык: Английский

Процитировано

11

Rhodium-Catalyzed Hydrolytic Cleavage of the Silicon–Carbon Bond of Silacyclobutanes to Access Silanols DOI

Wei-Ke Zhu,

Hua‐Jie Zhu,

Xiao‐Jun Fang

и другие.

Organic Letters, Год журнала: 2023, Номер 25(39), С. 7186 - 7191

Опубликована: Сен. 27, 2023

Herein, we report the first rhodium-catalyzed hydrolytic cleavage of silicon–carbon bond in silacyclobutanes using water as reactant. A series could be employed this reaction presence Rh/BINAP complex, resulting corresponding silanols good yields. Additionally, a chiral 1,1,4,4-tetraaryl-2,3-O-isopropylidene-l-threitol-derived phosphoramidite ligand used to yield Si-stereogenic silanol with promising enantioselectivity.

Язык: Английский

Процитировано

10

Metal-free three-component amino- and carbotrideuteromethylthiolation of alkenes in water DOI

Siyu Han,

Lin Zhao, Xinyu Zhou

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(21), С. 6064 - 6068

Опубликована: Янв. 1, 2024

Three-component amino- and carbotrideuteromethylthiolation of alkenes in water.

Язык: Английский

Процитировано

3

Copper-Catalyzed Synthesis of S–S Bond-Containing Silanols from SCBs and Trisulfide-1,1-dioxides DOI
Ying Chen, Fei Wang, Weidong Rao

и другие.

The Journal of Organic Chemistry, Год журнала: 2023, Номер 88(13), С. 7953 - 7961

Опубликована: Май 26, 2023

In this work, an efficient method for the copper-catalyzed ring-opening hydrolysis of silacyclobutanes to silanols was developed. This strategy has advantages friendly reaction conditions, simple operation, and good functional group compatibility. No additional additives are required in reaction, S-S bond can also be introduced into organosilanol compounds one step. Furthermore, success at gram scale demonstrates great potential developed protocol practical industrial applications.

Язык: Английский

Процитировано

8

Unveiling the electron-acceptor effect in selenium-doped Cu-N-C catalyst with atomically dispersed active sites for boosting Hg0 oxidation DOI

Linzhi Shen,

Ziwen Xiong,

Zhaohui Du

и другие.

Separation and Purification Technology, Год журнала: 2023, Номер 334, С. 126078 - 126078

Опубликована: Дек. 19, 2023

Язык: Английский

Процитировано

6

Selenosulfones, a Meetup of Chalcogens: A Journey Into Their Recent Chemistry DOI Creative Commons
Luana Bagnoli, Ornelio Rosati, Francesca Marini

и другие.

European Journal of Organic Chemistry, Год журнала: 2024, Номер 27(23)

Опубликована: Апрель 25, 2024

Abstract A mini review focused on the chemistry of selenosulfones reported since 2019 is here presented. Initially, methods aimed to preparation such moiety are discussed. Successively 1,2‐, 1,3‐, 1,4‐ and 1,7‐addition reactions C−C single multiple bonds illustrated. The forth chapter focuses electrophilic aromatic substitutions. fifth deals with C−H functionalizations while sixth one shows aryl diazonium salts or its precursors. radical coupling redox active reagents, subject section seventh. Selenosulfones challenged in nucleophilic substitutions phosphorus‐containing compounds shown eight nine followed by conclusions perspectives section.

Язык: Английский

Процитировано

2

Synthesis of Dihydrobenzosiloles and Silacyclopentanes by Double Hydroalumination of Terminal Alkynes DOI
Hidenori Kinoshita,

Ryusei Osawa,

Kotaro Ogihara

и другие.

Synlett, Год журнала: 2024, Номер unknown

Опубликована: Май 18, 2024

Abstract We have developed an efficient method for the synthesis of 2,3-dihydro-1H-1-benzosiloles in 19% to 90% isolated yield from 1-hydrosilyl-2-ethynylbenzenes by using two equivalents diisobutylaluminum hydride. The reaction mechanism involves regioselective double hydroalumination alkyne moiety followed cyclization a 2-alanyldihydrobenzosilole. A silacyclopentane (silolane) was also synthesized 97% corresponding 4-silylbut-1-yne under same conditions. Although substrate-scope study conducted on 0.5-mmol scale, gram-scale (2-ethynylphenyl)(diphenyl)silane optimized conditions successfully afforded desired product 94% without loss reactivity.

Язык: Английский

Процитировано

2