σ-Chelation-directed C–H functionalizations using Pd(ii) and Cu(ii) catalysts: regioselectivity, stereoselectivity and catalytic turnover
Top Cited Papers
- 16 October 2006
- journal article
- review article
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 4 (22), 4041-4047
- https://doi.org/10.1039/b611094k
Abstract
Recent progress in σ-chelation directed C–H functionalization from the authors' group is described to illustrate the challenges and opportunities in the development of synthetically-useful catalytic reactions involving C–H activation as the key step. Emphasis is placed on strategies for developing catalysis under mild conditions and controlling regio- and stereoselectivity.Keywords
This publication has 66 references indexed in Scilit:
- Synthesis of β-Boswellic Acid Analogues with a Carboxyl Group at C-17 Isolated from the Bark of Schefflera octophyllaThe Journal of Organic Chemistry, 2000
- Efficient Activation of Aromatic C-H Bonds for Addition to C-C Multiple BondsScience, 2000
- Transition Metal Catalyzed Coupling Reactions under C−H ActivationAngewandte Chemie International Edition, 1999
- Efficient catalytic addition of aromatic carbon-hydrogen bonds to olefinsNature, 1993
- Tilden Lecture. Selectivity and mechanism in catalytic asymmetric synthesisChemical Society Reviews, 1993
- Functionalisation of unactivated methyl groups through cyclopalladation reactionsTetrahedron, 1985
- Cyclopalladated Complexes in Organic SynthesisSynthesis, 1985
- Substitution at the 4-methyl of lanost-8-en-3-oneJournal of the Chemical Society, Chemical Communications, 1984
- Mechanism and Stereoselectivity of Asymmetric HydrogenationScience, 1982
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980