6533b856fe1ef96bd12b28a3

RESEARCH PRODUCT

A catalytic highly enantioselective direct synthesis of 2-bromo-2-nitroalkan-1-ols through a Henry reaction.

Victor Hernandez‐olmosGonzalo BlayJosé R. Pedro

subject

Nitroaldol reactionEnrichedCondensationPyridinesBromonitromethaneUNESCO::QUÍMICACatalytic ; Synthesis ; Henry reaction ; Enriched ; CondensationMolecular Conformationchemistry.chemical_elementAcetatesLigands:QUÍMICA [UNESCO]CatalysisCatalysisSynthesisMaterials ChemistryOrganic chemistryCatalyticAldehydesEthaneChemistryUNESCO::QUÍMICA::Química inorgánicaCondensationMetals and AlloysEnantioselective synthesisStereoisomerismGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Nitro CompoundsCopperPyridine ligandSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAlcoholsCeramics and CompositesHenry reactionCopper

description

Highly enantiomerically enriched 2-bromo-2-nitroalkan-1-ols are prepared by direct condensation of aliphatic and aromatic aldehydes with bromonitromethane in the presence of a catalytic amount of copper(II) acetate and a C1-symmetric camphorderived amino pyridine ligand. Blay Llinares, Gonzalo, Gonzalo.Blay@uv.es ; Hernandez Olmos, Victor, Victor.Hernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es

yearjournalcountryeditionlanguage
2008-10-03Chemical communications (Cambridge, England)
10.1039/b809739ahttps://pubmed.ncbi.nlm.nih.gov/18830511