TY - JOUR
T1 - Walking Metals for Remote Functionalization
AU - Sommer, Heiko
AU - Julia-Hernandez, Francisco
AU - Martin, Ruben
AU - Marek, Ilan
N1 - Funding Information: We thank ICIQ, European Research Council under the Seventh Framework Program of the European Community for the Israeli PI (ERC Grant Agreement 338912) and MINECO (CTQ2015-65496-R & Severo Ochoa Accreditation SEV-2013-0319) for financial support. I.M. is holder of the Sir Michael and Lady Sobell Academic Chair. H.S. acknowledges the Max-Planck-Society for a Minerva Fellowship. Publisher Copyright: © 2018 American Chemical Society.
PY - 2018/2/28
Y1 - 2018/2/28
N2 - The distant and selective activation of unreactive C-H and C-C bonds remains one of the biggest challenges in organic chemistry. In recent years, the development of remote functionalization has received growing interest as it allows for the activation of rather challenging C-H and C-C bonds distant from the initiation point by means of a "metal-walk". A "metal-walk" or "chain-walk" is defined by an iterative series of consecutive 1,2- or 1,3-hydride shifts of a metal complex along a single hydrocarbon chain. With this approach, simple building blocks or mixtures thereof can be transformed into complex scaffolds in a convergent and unified strategy. A variety of catalytic systems have been developed and refined over the past decade ranging from late-transition-metal complexes to more sustainable iron- and cobalt-based systems. As the possibilities of this field are slowly unfolding, this area of research will contribute considerably to provide solutions to yet unmet synthetic challenges.
AB - The distant and selective activation of unreactive C-H and C-C bonds remains one of the biggest challenges in organic chemistry. In recent years, the development of remote functionalization has received growing interest as it allows for the activation of rather challenging C-H and C-C bonds distant from the initiation point by means of a "metal-walk". A "metal-walk" or "chain-walk" is defined by an iterative series of consecutive 1,2- or 1,3-hydride shifts of a metal complex along a single hydrocarbon chain. With this approach, simple building blocks or mixtures thereof can be transformed into complex scaffolds in a convergent and unified strategy. A variety of catalytic systems have been developed and refined over the past decade ranging from late-transition-metal complexes to more sustainable iron- and cobalt-based systems. As the possibilities of this field are slowly unfolding, this area of research will contribute considerably to provide solutions to yet unmet synthetic challenges.
UR - https://www.scopus.com/pages/publications/85042693146
U2 - 10.1021/acscentsci.8b00005
DO - 10.1021/acscentsci.8b00005
M3 - Article
SN - 2374-7943
VL - 4
SP - 153
EP - 165
JO - ACS Central Science
JF - ACS Central Science
IS - 2
ER -