Synthesis 2014; 46(21): 2884-2896
DOI: 10.1055/s-0034-1379216
short review
© Georg Thieme Verlag Stuttgart · New York

Hydroaminoalkylation: Early-Transition-Metal-Catalyzed α-Alkylation of Amines

Eugene Chong
Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, BC, V6T 1Z1, Canada   Fax: +1(604)8222847   Email: schafer@chem.ubc.ca
,
Pierre Garcia
Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, BC, V6T 1Z1, Canada   Fax: +1(604)8222847   Email: schafer@chem.ubc.ca
,
Laurel L. Schafer*
Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, BC, V6T 1Z1, Canada   Fax: +1(604)8222847   Email: schafer@chem.ubc.ca
› Author Affiliations
Further Information

Publication History

Received: 21 July 2014

Accepted after revision: 04 September 2014

Publication Date:
06 October 2014 (online)


Abstract

The recent development and progress of early-transition-metal-catalyzed C–H alkylation adjacent to nitrogen of unprotected amines with alkenes are summarized. Group 4 and 5 metal complexes are very effective for hydroaminoalkylation catalysis, an emerging atom-economic C(sp3)–C(sp3) bond formation strategy.

1 Introduction

2 Group 4 Hydroaminoalkylation Catalysis

2.1 Intramolecular Hydroaminoalkylation

2.2 Intermolecular Hydroaminoalkylation

3 Group 5 Hydroaminoalkylation Catalysis

4 Conclusions and Outlook