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Early transition metal-catalyzed C-H alkylation: hydroaminoalkylation for C sp 3 -C sp 3 bond formation in the synthesis of selectively substituted amines.
- Source :
-
Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2018 Nov 06; Vol. 54 (89), pp. 12543-12560. - Publication Year :
- 2018
-
Abstract
- Hydroaminoalkylation is a 100% atom economic method for forming Csp3-Csp3 bonds through C-H activation α to an amine and subsequent reaction with an alkene. When catalyzed by early transition metals, this reaction allows for alternative disconnections for the synthesis of structurally complex amines. This method avoids the installation of protecting groups or directing groups and does not require added oxidants, or photoredox catalysts. In this feature article, we discuss the various selectively substituted amines that can be accessed by hydroaminoalkylation, with a special focus on the development of early transition metal catalysts for their rapid, step and atom efficient assembly.
Details
- Language :
- English
- ISSN :
- 1364-548X
- Volume :
- 54
- Issue :
- 89
- Database :
- MEDLINE
- Journal :
- Chemical communications (Cambridge, England)
- Publication Type :
- Academic Journal
- Accession number :
- 30334025
- Full Text :
- https://doi.org/10.1039/c8cc06445h