Muñiz
Research group
Abstract
The Muñiz group has continued with its efforts to develop sustainable synthetic methodology for advanced oxidative transformation of organic molecules. For 2015, 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 molecular iodine catalysis.
Topics addressed
- Metal-free boryation by hypervalent iodine chemistry
- Iodine-catalysed aliphatic C-H amination
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