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- Publications
- Influence
Iron-catalysed carbon-heteroatom and heteroatom-heteroatom bond forming processes.
- Arkaitz Correa, O. García Mancheño, C. Bolm
- Chemistry, Medicine
- Chemical Society reviews
- 22 May 2008
Given its ready availability, low price and environmentally friendly character, iron is an attractive and often advantageous alternative to other transition metals in the field of catalysis. This… Expand
TEMPO oxoammonium salt-mediated dehydrogenative Povarov/oxidation tandem reaction of N-alkyl anilines.
- H. Richter, O. García Mancheño
- Chemistry, Medicine
- Organic letters
- 18 October 2011
The synthesis of a variety of substituted quinolines from N-alkyl anilines by a one-pot dehydrogenative Povarov/oxidation tandem reaction with mono- and 1,2-disubstituted aryl and alkyl olefins was… Expand
Mild metal-free tandem α-alkylation/cyclization of N-benzyl carbamates with simple olefins.
- H. Richter, R. Froehlich, Constantin-Gabriel Daniliuc, O. García Mancheño
- Medicine, Chemistry
- Angewandte Chemie
- 20 August 2012
Easy does it! The chemoselective oxidative α-C(sp(3))-H alkylation/cyclization reaction of N-benzyl carbamates using simple mono-, di-, and trisubstituted olefins provides functionalized… Expand
Iron-catalyzed oxidative tandem reactions with TEMPO oxoammonium salts: synthesis of dihydroquinazolines and quinolines.
- Renate Rohlmann, T. Stopka, H. Richter, O. García Mancheño
- Chemistry, Medicine
- The Journal of organic chemistry
- 7 June 2013
A straightforward iron-catalyzed divergent oxidative tandem synthesis of dihydroquinazolines and quinolines from N-alkylanilines using a TEMPO oxoammonium salt as a mild and nontoxic oxidant has been… Expand
Catalyzed selective direct α- and γ-alkylation of aldehydes with cyclic benzyl ethers by using T(+)BF4- in the presence of an inexpensive organic acid or anhydride.
- H. Richter, Renate Rohlmann, O. García Mancheño
- Medicine, Chemistry
- Chemistry
- 4 October 2011
The cross dehydrogenative coupling (CDC) of cyclic benzyl ethers with aliphatic and α,β-unsaturated aldehydes has been developed. The mild reaction conditions, in which an N-oxoammonium salt derived… Expand
Chiral copper complexes of phosphino sulfenyl ferrocenes as efficient catalysts for enantioselective formal Aza Diels-Alder reactions of N-sulfonyl imines.
- O. García Mancheño, R. Gómez Arrayás, J. Carretero
- Chemistry, Medicine
- Journal of the American Chemical Society
- 21 January 2004
In the presence of a catalytic amount of silver perchlorate, copper(I) bromide complexes of planar chiral 1-phosphino-2-sulfenylferrocenes behave as very efficient chiral Lewis acids catalysts in the… Expand
Highly Enantioselective Nucleophilic Dearomatization of Pyridines by Anion-Binding Catalysis.
- O. García Mancheño, Soeren Asmus, Mercedes Zurro, T. Fischer
- Chemistry, Medicine
- Angewandte Chemie
- 20 July 2015
The asymmetric dearomatization of N-heterocycles is an important synthetic method to gain bioactive and synthetically valuable chiral heterocycles. However, the catalytic enantio- and regioselective… Expand
1-Phosphino-2-sulfenylferrocenes as planar chiral ligands in enantioselective palladium-catalyzed allylic substitutions.
- O. García Mancheño, J. Priego, S. Cabrera, R. Gómez Arrayás, T. Llamas, J. Carretero
- Chemistry, Medicine
- The Journal of organic chemistry
- 9 April 2003
The synthesis of a wide structural variety of enantiopure 1-phosphino-2-sulfenylferrocene ligands 1 possessing exclusively planar chirality is described. In the case of the readily available… Expand
"Click" bis-triazoles as neutral C-H···anion-acceptor organocatalysts.
- Stephan Beckendorf, Soeren Asmus, C. Mück-Lichtenfeld, O. García Mancheño
- Chemistry, Medicine
- Chemistry
- 28 January 2013
Chiral Triazoles in Anion-Binding Catalysis: New Entry to Enantioselective Reissert-Type Reactions.
- Mercedes Zurro, Soeren Asmus, J. Bamberger, Stephan Beckendorf, O. García Mancheño
- Chemistry, Medicine
- Chemistry
- 7 March 2016
Easily accessible and tunable chiral triazoles have been introduced as a novel class of C-H bond-based H-donors for anion-binding organocatalysis. They have proven to be effective catalysts for the… Expand