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Sulfur in Waste‐Free Sustainable Synthesis: Advancing Carbon‐Carbon Coupling Techniques Review

Journal Angewandte Chemie International Edition
ISSN: 1433-7851 , E-ISSN: 1521-3773
Output data Year: 2024, Volume: 63, Number: 18, Article number : e202402109, Pages count : DOI: 10.1002/anie.202402109
Authors Nikita Shlapakov 1 , Andrey Kobelev 1 , Julia Burykina 1 , Cheng Yuan-Zheng 2 , You Shu-Li 2 , Ananikov Valentine P. 1
Affiliations
1 Zelinsky Institute of Organic Chemistry Russian Academy of Sciences Leninsky Prospekt 47 119991 Moscow RUSSIAN FEDERATION
2 Chinese Academy of Sciences Shanghai Institute of Organic Chemistry Chemistry RUSSIAN FEDERATION

Abstract: This review explores the pivotal role of sulfur in advancing sustainable carbon-carbon (C−C) coupling reactions. The unique electronic properties of sulfur, as a soft Lewis base with significant mesomeric effect make it an excellent candidate for initiating radical transformations, directing C−H-activation, and facilitating cycloaddition and C−S bond dissociation reactions. These attributes are crucial for developing waste-free methodologies in green chemistry. Our mini-review is focused on existing sulfur-directed C−C coupling techniques, emphasizing their sustainability and comparing state-of-the-art methods with traditional approaches. The review highlights the importance of this research in addressing current challenges in organic synthesis and catalysis. The innovative use of sulfur in photocatalytic, electrochemical and metal-catalyzed processes not only exemplifies significant advancements in the field but also opens new avenues for environmentally friendly chemical processes. By focusing on atom economy and waste minimization, the analysis provides broad appeal and potential for future developments in sustainable organic chemistry.
Cite: Nikita Shlapakov , Andrey Kobelev , Julia Burykina , Cheng Y-Z. , You S-L. , Ananikov V.P.
Sulfur in Waste‐Free Sustainable Synthesis: Advancing Carbon‐Carbon Coupling Techniques
Angewandte Chemie International Edition. 2024. V.63. N18. e202402109 . DOI: 10.1002/anie.202402109 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:001190646200001
Scopus: 2-s2.0-85188548375
OpenAlex: W4392297234
Citing: Пока нет цитирований
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