Synlett 2015; 26(15): 2088-2098
DOI: 10.1055/s-0034-1381031
account
© Georg Thieme Verlag Stuttgart · New York

Advances in Transition-Metal-Catalyzed Direct sp3-Carbon–Hydrogen Bond Functionalization

Wei Zhang
a   Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. of China   Email: nxwang@mail.ipc.ac.cn
,
Nai-Xing Wang*
a   Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. of China   Email: nxwang@mail.ipc.ac.cn
,
Yalan Xing*
b   Department of Chemistry, William Paterson University of New Jersey, 300 Pompton Road, Wayne NJ 07470, USA   Email: xingy@wpunj.edu
› Author Affiliations
Further Information

Publication History

Received: 27 March 2015

Accepted after revision: 26 May 2015

Publication Date:
21 August 2015 (online)


Abstract

Transition-metal-catalyzed direct carbon–hydrogen bond functionalization has made significant advances in the field of carbon–hydrogen bond activation over the past decades. This methodology has the potential to be used in many different areas of chemistry; for example, it can provide an opportunity for the synthesis of various kinds of complex compounds. This account mainly focuses on recent advances in transition-metal-catalyzed direct sp3-carbon–hydrogen bond functionalization to form carbon–carbon bonds.

1 Introduction

2 Carbon–Carbon Bond Formation via Direct sp3-Carbon–Hydrogen Bond Functionalization

2.1 Coupling of sp3-Carbon–Hydrogen and sp-Carbon–Hydrogen Bonds

2.2 Coupling of sp3-Carbon–Hydrogen and sp2-Carbon–Hydrogen Bonds

2.3 Coupling of sp3-Carbon–Hydrogen and sp3-Carbon–Hydrogen Bonds

2.4 Coupling of sp3-Carbon–Hydrogen and C–X Bonds

3 Conclusion