Muñiz
Research group
Abstract
The Muñiz group devotes efforts to develop sustainable synthetic methodology for advanced oxidative transformation of organic molecules. For 2017, work in this area has provided new transformations that are based on molecular iodine reagents and catalysts. Prominent examples include pioneering work on enantioselective alkene diamination reactions under intermolecular reaction control and radical-based C-H amination reactions.
Topics addressed
- Iodine-catalysed deraomatisation
Articles
“Cooperative Light-Activated Iodine and Photoredox Catalysis for the Amination of Csp3-H Bonds “
Angew. Chem. 2017, 129, 8117-8121
Angew. Chem. Int. Ed. 2017, 56, 8004-8008
P. Becker, T. Duhamel, J. C. Stein, M. Reiher, K. Muñiz
“Catalytic Asymmetric Diamination of Styrenes“
J. Am. Chem. Soc. 2017, 139, 4354-4357
K. Muñiz, L. Barreiro, R. M. Romero, C. Martínez
“Selective Piperidine Synthesis Exploiting Iodine-Catalyzed Csp3-H Amination under Visible Light “
ACS Catal. 2017, 7, 4122-4125
H. Zhang, K. Muñiz
“Enantioselective 4-Hydroxylation of Phenols under Chiral Organoiodine(I/III) Catalysis “
Synthesis 2017, 49, 2901-2906
K. Muñiz, L. Fra
“Vicinal Difunctionalization of Alkenes under Iodine(III) Catalysis involving Lewis Base Adducts “
Adv. Synth. Catal. 2017, 359, 1290-1294
K. Aertker, R. J. Rama, J. Oppalach, K. Muñiz