Pd(II)-Catalyzed C–H Iodination Using Molecular I2 as the Sole Oxidant
Journal of the American Chemical Society2013Vol. 135(28), pp. 10326–10329
Citations Over TimeTop 1% of 2013 papers
Abstract
Pd-catalyzed ortho-C-H iodination directed by a weakly coordinating amide auxiliary using I2 as the sole oxidant was developed. This reaction is compatible with a wide range of heterocycles including pyridines, imidazoles, oxazoles, thiazoles, isoxazoles, and pyrazoles.
Related Papers
- → Fast Halogenation of Some N‐Heterocycles by Means of N,N′‐Dihalo‐5,5‐dimethylhydantoin(2013)30 cited
- → Highly efficient and recyclable catalyst for the direct chlorination, bromination and iodination of terminal alkynes(2017)14 cited
- → Unprecedented Halogenation of Biginelli Compounds of Salicyldehyde(2013)2 cited
- → 601. Quantitative aspects of the base-catalysed halogenation of aliphatic ketones. Part III. Comparison of bromination and iodination(1957)4 cited
- → Halogenation and Dehalogenation of the 2,7‐Naphthyridine Ring.(2002)1 cited