Stereoselective Domino Carbocyclizations of γ- And δ-Cyano-N-tosylhydrazones with Alkenylboronic Acids with Formation of Two Different C(sp3)-C(sp2) Bonds on a Quaternary Stereocenter

Journal of the American Chemical Society

Volumn 138, Issue 37, 2016, Pages 12061-12064

  Plaza, Manuel ^a   Valdés, Carlos ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

KETONES; MICROWAVE IRRADIATION;

CARBOCYCLIZATION; DIASTEREO-SELECTIVITY; EXPERIMENTAL CONDITIONS; N-TOSYLHYDRAZONES; NOVEL STRATEGIES; QUATERNARY STEREOCENTERS; STEREO-SELECTIVE; STRUCTURAL MODIFICATIONS;

STEREOSELECTIVITY;

ANDROSTERONE; BORONIC ACID DERIVATIVE; DIOXANE; HYDRAZONE DERIVATIVE; KETONE DERIVATIVE;

ARTICLE; CATALYST; COVALENT BOND; CYCLIZATION; HEATING; HYDROLYSIS; MICROWAVE IRRADIATION; NUCLEOPHILICITY; REACTION TIME; STEREOISOMERISM; STEREOSELECTIVITY; SYNTHESIS;

EID: 84988662342     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.6b08116     Document Type: Article

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