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Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2013, Volume 52, Issue 49, pp. 12942 - 12945
Fully loaded: A coordinating activation strategy has been developed to furnish α‐quaternary α‐amino acids through the iron(III)‐catalyzed oxidative... 
iron | homogeneous catalysis | cross‐coupling | α‐quaternary α‐amino acids | coordinating activation | cross-coupling | α-quaternary α-amino acids | Oxidation-Reduction | Esters - chemistry | Amino Acids - chemistry | Ferric Compounds - chemistry | Molecular Structure | Amino Acids - chemical synthesis | Catalysis | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 03/2016, Volume 113, Issue 11, pp. E1452 - E1459
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 03/2010, Volume 132, Issue 8, pp. 2719 - 2728
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2015, Volume 54, Issue 31, pp. 8961 - 8965
...′‐aryl urea derivatives ligated to pseudoephedrine as a chiral auxiliary. In situ silylation and enolization induces diastereoselective migration of the N′‐aryl group to the α... 
chiral auxiliaries | enolates | amino acids | pseudoephedrine | arylation | Amino Acids - chemistry | Molecular Structure | Pseudoephedrine - chemistry | Stereoisomerism | Index Medicus | Asymmetry | Migration | Hydantoin | Electronics | Amino acids | Ureas | Derivatives | Rings (mathematics)
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 05/2015, Volume 357, Issue 8, pp. 1909 - 1918
...‐carboxylation of para‐hydroxystyrene derivatives with excellent regio‐ and (E/Z)‐stereoselectivity by exclusively acting at the β... 
enzyme catalysis | para-hydroxystyrenes | biotransformations | regioselective carboxylation | reaction mechanism | phenolic acid decarboxylases | Regioselective carboxylation | Reaction mechanism | Enzyme catalysis | Biotransformations | Phenolic acid decarboxylases | Full Paper | Full Papers | para‐hydroxystyrenes
Journal Article