Novel Acetoxylation and C−C Coupling Reactions at Unactivated Positions in α-Amino Acid Derivatives
Top Cited Papers
- 27 June 2006
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 8 (15), 3391-3394
- https://doi.org/10.1021/ol061389j
Abstract
Under special conditions, N-phthaloyl-α-amino acid amides of 8-aminoquinoline can be either acetoxylated or arylated selectively at the β-carbon. In certain cases, arylation can be effected at the γ-carbon.Keywords
This publication has 13 references indexed in Scilit:
- Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O2 as an OxidantJournal of the American Chemical Society, 2006
- Pd‐Catalyzed Stereoselective Oxidation of Methyl Groups by Inexpensive Oxidants under Mild Conditions: A Dual Role for Carboxylic Anhydrides in Catalytic C-H Bond OxidationAngewandte Chemie International Edition, 2005
- Highly Regioselective Arylation of sp3 C−H Bonds Catalyzed by Palladium AcetateJournal of the American Chemical Society, 2005
- Palladium‐Catalyzed Asymmetric Iodination of Unactivated C-H Bonds under Mild ConditionsAngewandte Chemie International Edition, 2005
- Transition metal-catalyzed carbon–carbon bond activationChemical Society Reviews, 2004
- Palladium-Catalyzed Oxygenation of Unactivated sp3 C−H BondsJournal of the American Chemical Society, 2004
- A Highly Selective Catalytic Method for the Oxidative Functionalization of C−H BondsJournal of the American Chemical Society, 2004
- Oxidation of unactivated methyl groups via a cyclopalladation reactionJournal of the Chemical Society, Chemical Communications, 1985
- Substitution at the 4-methyl of lanost-8-en-3-oneJournal of the Chemical Society, Chemical Communications, 1984
- Palladation of dimethylhydrazones, oximes, and oxime O-allyl ethers: crystal structure of [Pd3(ON = CPriPh)6]Journal of the Chemical Society, Chemical Communications, 1978