Highly stereoselective synthesis of tertiary propargylic centers and their isomerization to enantiomerically enriched allenes

Chemistry - A European Journal

Volumn 18, Issue 32, 2012, Pages 9775-9779

  García Ruano, José Luis ^a   Marzo, Leyre ^a   Marcos, Vanesa ^a   Alvarado, Cuauhtémoc ^a   Alemán, José ^a  

^a UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

Author keywords

allenes; anti michael addition; propargylic centers; sulfonylacetylenes; sulfoxides

Indexed keywords

ALLENES; ANTI-MICHAEL ADDITION; PROPARGYLIC CENTERS; SULFONYLACETYLENES; SULFOXIDES;

ADDITION REACTIONS; ENANTIOMERS; FUNCTIONAL GROUPS; ISOMERIZATION; LITHIUM; STEREOCHEMISTRY; STEREOSELECTIVITY;

HYDROCARBONS;

ALKADIENE; DRUG DERIVATIVE; PARGYLINE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; ISOMERISM; STEREOISOMERISM; SYNTHESIS;

ALKADIENES; ISOMERISM; MOLECULAR STRUCTURE; PARGYLINE; STEREOISOMERISM;

EID: 84864444662     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201201607     Document Type: Article

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