Advancements in Chan-Lam cross-coupling reactions utilizing copper and nickel salts, Cu/Ni-incorporated polymers, and nanocomposites DOI
Palani Sasikumar‬‬‬‬, Anjoy Majhi

Inorganic Chemistry Communications, Journal Year: 2024, Volume and Issue: unknown, P. 113799 - 113799

Published: Dec. 1, 2024

Language: Английский

The green chemistry paradigm in modern organic synthesis DOI
Sergei G. Zlotin, Ksenia S. Egorova, Valentine P. Ananikov

et al.

Russian Chemical Reviews, Journal Year: 2023, Volume and Issue: 92(12), P. RCR5104 - RCR5104

Published: Dec. 1, 2023

After the appearance of green chemistry concept, which was introduced in vocabulary early 1990s, its main statements have been continuously developed and modified. Currently, there are 10–12 cornerstones that should form basis for an ideal chemical process. This review analyzes accumulated experience achievements towards design products processes reduce or eliminate use generation hazardous substances. The presents views leading Russian scientists specializing various fields this subject, including homogeneous heterogeneous catalysis, fine basic organic synthesis, electrochemistry, polymer chemistry, based on bio-renewable feedstocks energetic compounds materials. A new approach to quantitative evaluation environmental friendliness by authors is described. <br> bibliography includes 1761.

Language: Английский

Citations

39

Recent advances in Chan–Lam coupling reaction DOI
P. Devi, Salim Saranya, Gopinathan Anilkumar

et al.

Catalysis Science & Technology, Journal Year: 2024, Volume and Issue: 14(9), P. 2320 - 2351

Published: Jan. 1, 2024

Chan–Lam coupling has evolved as a shining star among C–heteroatom reactions because of its greener open flask chemistry and tremendous possibilities in terms substrate bank, catalyst varieties, unlocking nature friendly conditions, etc.

Language: Английский

Citations

10

Transition metal-free C(sp3)–H selenation of β-ketosulfones DOI

Dilshat Abdukerem,

Hui Chen,

Zechuan Mao

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(10), P. 2075 - 2080

Published: Jan. 1, 2024

Direct C(sp 3 )-H selenation, which is most atom economical, remains a formidable challenge, and only few examples have been reported to date. In this article, we introduce the transition metal-free selenation with β-ketosulfones diselenides as material source.

Language: Английский

Citations

4

Bio-decorated of copper nanoparticles over Arabic gum modified magnetic nanoparticles: Its catalytic activity for C-S coupling reactions DOI

Waqid Al-Mussawi,

Ali B. Abou Hammad, Suranjana V. Mayani

et al.

Journal of Organometallic Chemistry, Journal Year: 2025, Volume and Issue: unknown, P. 123669 - 123669

Published: April 1, 2025

Language: Английский

Citations

0

Synthesis of β‐Hydroxyselenides via Electrochemical Hydroxyselenenylation of Alkenes with Diselenides and H2O DOI
Weiwei Li, Yingyuan Hu,

Junsheng Hou

et al.

ChemistrySelect, Journal Year: 2024, Volume and Issue: 9(5)

Published: Feb. 2, 2024

Abstract A practical electrochemical method for the synthesis of β‐hydroxyselenides has been developed under an external oxidant‐free condition at room temperature air from alkenes with diselenides and H 2 O. radical mechanism is proposed this transformation gram‐scale reactions demonstrate practicability reaction.

Language: Английский

Citations

3

The Reaction of Aryl Thiols or Thioureas with o‐Diiodoarenes/NaH to Access o‐Iodoaryl Thioethers DOI

Min Hu,

Dianfan Liu,

Yuan Liu

et al.

Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: 366(7), P. 1538 - 1544

Published: Feb. 8, 2024

Abstract Herein we report a method for the synthesis of thioethers by forging C(aryl)‐S bond via an aryne mechanism. The active species can be generated from o ‐diiodoarenes and NaH in THF at room temperature, then lead to arylations wide range aryl thiols thioureas. Different transition metal‐catalyzed cross‐coupling reactions, no disubstituted byproduct is formed our protocol. ‐iodoaryl thioether products are intermediates that could transformed into pharmaceutically interesting molecules.

Language: Английский

Citations

2

Deboronative Selenylation, Bromination, or Hydroxylation of Organic Boronic Acids Facilitated by Tetrabutylammonium Tribromide under Transition Metal-Free Conditions DOI
Yongsheng Tian,

Lanfeng Wei,

Jiawei Huang

et al.

Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(6), P. 1987 - 1987

Published: Jan. 1, 2024

Language: Английский

Citations

2

Electrochemically promoted selenocyclization for the synthesis of organoselenyl isoxazoles DOI
Nan Sun, Zhi Qiao,

Jiamin Li

et al.

Green Chemistry, Journal Year: 2024, Volume and Issue: 26(19), P. 10240 - 10246

Published: Jan. 1, 2024

Herein, we report a general and sustainable electrochemically promoted oxidative selenocyclization protocol for the synthesis of organoselenyl isoxazoles from 2-alkyn-1-one O -methyloximes diorganyl diselenides.

Language: Английский

Citations

2

Copper‐Mediated C−H Chalcogenation of Heterocycles: Application to the Synthesis of Chalcogenoxanthones DOI
Yunhao Zhou, Yue Xu, Tao Zheng

et al.

Advanced Synthesis & Catalysis, Journal Year: 2023, Volume and Issue: 365(19), P. 3353 - 3359

Published: Aug. 16, 2023

Abstract A copper‐mediated C( sp 2 )−H chalcogenation of heterocycles with readily available dichalcogenide, benzeneselenol and thiol is described. This protocol demonstrates scalability, good chemo‐ regio‐selectivity, as well broad functional group tolerance, which overall provides an accessible method to valuable aryl chalcogenides. The chalcogenated picolinamide products could be further transformed into selenoxanthones thioxanthone scaffolds through intramolecular cyclization via a semi‐one pot process.

Language: Английский

Citations

5

Highly efficient synthesis of arylsulide derivatives from coupling reaction of aryl titanium reagents with N-aryl thiosuccinimides catalyzed by copper under ligand-free conditions DOI
Zhihao Zhang,

Jiaxia Pu,

Xiao-Ying Jia

et al.

Journal of Organometallic Chemistry, Journal Year: 2024, Volume and Issue: 1014, P. 123192 - 123192

Published: May 21, 2024

Language: Английский

Citations

1