Chemo-, regio- and stereoselective synthesis of 2-alkylidene-5- hydroxymethyl-hydrofurans by cyclization of 1,3-dicarbonyl-dianions with 1- bromo-2,3-epoxypropanes

Synlett

Volumn , Issue 4, 2000, Pages 501-503

  Langer, Peter ^a   Freifeld, Ilya ^a   Holtz, Edith ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

Ambident dianions; Cyclization reactions; Epoxides; Regioselectivity; Stereoselective syntheses

Indexed keywords

ALKADIENE; EPOXIDE; FURAN DERIVATIVE; PROPANE;

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

EID: 0034029616     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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26. 4: C 58.05, H 7.58; found C 58.24, H 7.42. All compounds were prepared as racemic material and gave satisfactory spectroscopic and analytical and/ or high resolution mass data.
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