Merging domino and redox chemistry: Stereoselective access to di- and trisubstituted β,γ-unsaturated acids and esters

Chemistry - A European Journal

Volumn 18, Issue 12, 2012, Pages 3468-3472

  Tejedor, David ^a   Méndez Abt, Gabriela ^a   Cotos, Leandro ^a   García Tellado, Fernando ^a  

^a INSTITUTO DE PRODUCTOS NATURALES Y AGROBIOLOGÍA   (Spain)

Author keywords

alkenes; domino reactions; redox chemistry; stereoselectivity; water

Indexed keywords

DOMINO REACTIONS; MALONATES; PROPARGYL; REDOX CHEMISTRY; STEREO-SELECTIVE; STEREOSELECTIVE SYNTHESIS; UNSATURATED ACIDS; VINYL ETHERS; WATER AS SOLVENT;

CARBOXYLIC ACIDS; ESTERIFICATION; ESTERS; ETHERS; MERGING; METHANOL; OLEFINS; ORGANIC SOLVENTS; REACTION KINETICS; REDOX REACTIONS; STEREOCHEMISTRY; WATER;

STEREOSELECTIVITY;

ALKENE; CARBOXYLIC ACID; ESTER; SOLVENT; WATER;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; MICROWAVE RADIATION; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

ALKENES; CARBOXYLIC ACIDS; ESTERS; MICROWAVES; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; SOLVENTS; STEREOISOMERISM; WATER;

EID: 84859075770     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201103763     Document Type: Article

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