Unexpected stereoselective sodium acetate catalyzed multicomponent cyclization of aryl aldehydes, malononitrile and acetone into cis-4-dicyanomethylene-2,6-diarylcyclohexane-1,1-dicarbonitriles

Tetrahedron Letters

Volumn 48, Issue 38, 2007, Pages 6614-6619

  Elinson, Michail N ^a   Vereshchagin, Anatolii N ^a   Feducovich, Sergey K ^a   Zaimovskaya, Tatyana A ^b   Starikova, Zoya A ^c   Belyakov, Pavel A ^a   Nikishin, Gennady I ^a  

^a N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

^b TOPCHIEV INSTITUTE OF PETROCHEMICAL SYNTHESIS   (Russian Federation)

^c A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

Author keywords

2,6 Diarylcyclohexane 1,1 dicarbonitriles; Acetone; Aryl aldehydes; Catalysis; Malononitrile; Multicomponent reaction; Sodium acetate; Stereoselectivity

Indexed keywords

ACETIC ACID; ACETONE; ALDEHYDE; CYANIDE; CYCLOHEXANE DERIVATIVE; MALONONITRILE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 34548023093     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.07.119     Document Type: Article

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