O. García Mancheño

Publications28
h-index17
Citations1,720
Highly Influential Citations1
Claim Author Page
Author pages are created from data sourced from our academic publisher partnerships and public sources.

Recommended Authors

  • C. Bolm
  • 942 Publications, 29,317 Citations
  • E. Jacobsen
  • 453 Publications, 34,631 Citations
  • O. G. Mancheño
  • 96 Publications, 1,048 Citations
  • D. Nicewicz
  • 95 Publications, 6,054 Citations
  • Publications
  • Influence
Iron-catalysed carbon-heteroatom and heteroatom-heteroatom bond forming processes.
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
  • 752
  • 1
TEMPO oxoammonium salt-mediated dehydrogenative Povarov/oxidation tandem reaction of N-alkyl anilines.
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
  • 136
Mild metal-free tandem α-alkylation/cyclization of N-benzyl carbamates with simple olefins.
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
  • 80
Iron-catalyzed oxidative tandem reactions with TEMPO oxoammonium salts: synthesis of dihydroquinazolines and quinolines.
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
  • 99
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.
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
  • 72
Chiral copper complexes of phosphino sulfenyl ferrocenes as efficient catalysts for enantioselective formal Aza Diels-Alder reactions of N-sulfonyl imines.
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
  • 127
Highly Enantioselective Nucleophilic Dearomatization of Pyridines by Anion-Binding Catalysis.
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
  • 49
1-Phosphino-2-sulfenylferrocenes as planar chiral ligands in enantioselective palladium-catalyzed allylic substitutions.
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
  • 91
"Click" bis-triazoles as neutral C-H···anion-acceptor organocatalysts.
  • 35
Chiral Triazoles in Anion-Binding Catalysis: New Entry to Enantioselective Reissert-Type Reactions.
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
  • 39