Direct and highly regioselective and enantioselective allylation of β-diketones

Nature

Volumn 487, Issue 7405, 2012, Pages 86-89

  Chalifoux, Wesley A ^a   Reznik, Samuel K ^a   Leighton, James L ^a  

^a Columbia University ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIKETONE; 3 HYDROXYKETONE; BRONSTED ACID; KETONE; METHANOL; SPONGISTATIN 1; UNCLASSIFIED DRUG; ACETYLACETONE; ALKANONE; HYDROCHLORIC ACID; MACROLIDE; SILANE DERIVATIVE;

ACTIVATION ENERGY; ASYMMETRY; CHEMICAL ANALYSIS; KETONE;

ALLYLATION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOMER; ENANTIOSELECTIVITY; NUCLEOPHILICITY; PRIORITY JOURNAL; REGIOSELECTIVITY; SYNTHESIS; CHEMISTRY; METHODOLOGY; STEREOISOMERISM;

CHEMISTRY TECHNIQUES, SYNTHETIC; HYDROCHLORIC ACID; KETONES; MACROLIDES; METHANOL; PENTANONES; SILANES; STEREOISOMERISM;

EID: 84863438557     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/nature11189     Document Type: Article

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