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Synlett 2015; 26(13): 1785-1803
DOI: 10.1055/s-0034-1379912
DOI: 10.1055/s-0034-1379912
account
Hypervalent Iodine(III) in Direct Carbon–Hydrogen Bond Functionalization
Further Information
Publication History
Received: 10 February 2015
Accepted after revision: 18 March 2015
Publication Date:
20 May 2015 (online)
Abstract
Direct methods of novel bond formation through functionalization of nonreactive carbon–hydrogen bonds represent an efficient synthetic approach. Cross-dehydrogenative coupling has emerged as an area of huge potential and importance for novel bond formation. The application of hypervalent iodine(III) reagents in direct carbon–hydrogen bond functionalization reactions is of immense interest because the functionalization of the nonreactive carbon–hydrogen bonds proceeds under metal-free reaction conditions. This account covers recent developments in the area of hypervalent iodine(III) mediated direct carbon–hydrogen bond functionalization.
1 Introduction
2 Intramolecular Amination for Carbazole Synthesis
3 Intermolecular Amination
4 Intermolecular Annulation
5 Intermolecular Nucleophilic Amination
6 Hypervalent Iodine(III) Mediated Radical Reactions
6.1 Cross-Dehydrogenative Coupling of a Heterocycle and an Aldehyde
6.2 Cross-Dehydrogenative Coupling of a Heterocycle and an Alkane
6.3 Intramolecular Cyclization
7 Conclusion
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For a comprehensive review of transition-metal-free coupling reactions, see: