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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.

Authors :
Edwards PM
Schafer LL
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