Muñiz
Research group
Abstract
The Muñiz group has continued the development of new synthetic methodology for advanced oxidative amination of organic molecules. For 2014, work on this topic focussed on the realisation of economic transformations under environmentally benign metal-free conditions.
Major advances were made in the area of hypervalent iodine(III) chemistry and halogenated amide reagents.
Topics addressed
- Metal-free amination by hypervalent iodine chemistry
- Metal-mediated amination using copper reagents
Articles
“A Versatile Metal-Free Intermolecular Aminochlorination of Alkenes”
Adv. Synth. Catal. 2014, 356, 205
C. Martínez, K. Muñiz
“Copper-Mediated 1,4-Diamination of 1,3-Butadienes”
Eur. J. Org. Chem. 2014, 2017
C. Martínez, L. Martínez, J. Kirsch, E. C. Escudero-Adán, E. Martin, K. Muñiz
“Recent Progress in Vicinal Difunctionalization of Alkenes with Iodine(III) Reagents and Catalysts”
Chem. Asian J. 2014, 9, 972
M. Romero, T. H. Wöste, K. Muñiz
“Recent Progress in Vicinal Difunctionalization of Alkenes with Iodine(III) Reagents and Catalysts”
Org. Lett. 2013, 15, 1008
C. Röben, J. A. Souto, E. C. Escudero-Adán, K. Muñiz
“Indole Synthesis Based On A Modified Koser Reagent”
Angew. Chem. Int. Ed. 2014, 53, 7349
L. Fra, A. Millán, J. A. Souto, K. Muñiz
“Hypervalent Iodine Mediated Oxidative Amination of Allenes”
Org. Lett. 2014, 16, 4715
N. Purkait, S. Okamura, J. A. Souto, K. Muñiz