Distal radical migration strategy: an emerging synthetic means
The remote radical migration strategy has gained considerable momentum. During the past three years, we have witnessed the rapid development of sustainable and practical C-C and C-H bond functionalization by means of long-distance 1, n -radical migration ( n = 4, 5, 6) events. Its advent brings our...
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Veröffentlicht in: | Chemical Society reviews 2018-02, Vol.47 (3), p.654-667 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The remote radical migration strategy has gained considerable momentum. During the past three years, we have witnessed the rapid development of sustainable and practical C-C and C-H bond functionalization by means of long-distance 1,
n
-radical migration (
n
= 4, 5, 6) events. Its advent brings our chemical community a new platform to deal with the challenging migration transformations and thus complements the existing ionic-type migration protocols. In this review, the recent achievements in distal radical migration triggered C-C and C-H bond functionalization are summarized.
In the past three years, we have witnessed the rapid development of C-C and C-H bond functionalization by means of long-distance radical migration events which bring us a new platform to deal with the challenging C-C and C-H bond functionalization. |
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ISSN: | 0306-0012 1460-4744 |
DOI: | 10.1039/c7cs00507e |