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Recent advances in hydride transfer-involved C(sp3)–H activation reactions
The hydride transfer reaction, which is characterized by a redox-neutral and step/atom economic process, has emerged as an enabling platform for C(sp3)–H activation with high efficiency. During the past five years, significant advances have been made in new versions of hydride transfer-enabled C(sp3...
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Published in: | Organic chemistry frontiers an international journal of organic chemistry 2021-03, Vol.8 (6), p.1364-1383 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | The hydride transfer reaction, which is characterized by a redox-neutral and step/atom economic process, has emerged as an enabling platform for C(sp3)–H activation with high efficiency. During the past five years, significant advances have been made in new versions of hydride transfer-enabled C(sp3)–H activation, which mainly include the construction of novel scaffolds for cycles, and the intermolecular methods of both hydride transfer and C(sp3)–H functionalization. Herein, we summarize recent progress according to the reaction types categorized into hydride transfer/intramolecular C(sp3)–H functionalization, hydride transfer/intermolecular C(sp3)–H functionalization, and hydride reduction reactions. Furthermore, unsolved scientific problems as well as future directions in this field are also directly indicated. This review covers the period from 2016 to 2020. |
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ISSN: | 2052-4110 2052-4110 |
DOI: | 10.1039/d0qo01502d |