The use of carboxylic acids as traceless directing groups for regioselective C–H bond functionalisation
Open Access
- 28 April 2017
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 53 (41) , 5584-5597
Abstract
This feature article focuses on the use of carboxylic acids as traceless directing groups and the application of this concept to achieve regiochemical control in organic chemistry.Keywords
Funding Information
- Engineering and Physical Sciences Research Council (EP/L014017/2)
This publication has 56 references indexed in Scilit:
- Advances in the development of catalytic tethering directing groups for C–H functionalization reactionsOrganic & Biomolecular Chemistry, 2016
- Transition metal-catalyzed C–H bond functionalizations by the use of diverse directing groupsOrganic Chemistry Frontiers, 2015
- Recent advances in directed C–H functionalizations using monodentate nitrogen-based directing groupsOrganic Chemistry Frontiers, 2014
- Challenges in C–C bond formation through direct transformations of sp2 C–H bondsTetrahedron, 2012
- Towards mild metal-catalyzed C–H bond activationChemical Society Reviews, 2011
- Transition metal-catalyzed arylation of unactivated C(sp3)–H bondsChemical Society Reviews, 2011
- Removable Directing Groups in Organic Synthesis and CatalysisAngewandte Chemie International Edition, 2011
- Transition‐Metal‐Catalyzed Direct Arylation of (Hetero)Arenes by C-H Bond CleavageAngewandte Chemie International Edition, 2009
- Transition metal-catalyzed C–H activation reactions: diastereoselectivity and enantioselectivityChemical Society Reviews, 2009
- Palladium(II)‐Catalyzed C-H Activation/C-C Cross‐Coupling Reactions: Versatility and PracticalityAngewandte Chemie International Edition, 2009