Stereoselective syntheses of bridgehead hydroxy compounds via reductive cyclization reactions promoted by samarium diiodide

Article abstract of DOI:10.1080/00397919108021791

Cycloalkanones appended with an α,β-unsaturated carbonyl side chain react with 2.25 equivalents of samarium diiodide to form bicyclic or tricyclic bridgehead hydroxy compounds stereoselectivity in moderate yield.

Full text of DOI:10.1080/00397919108021791

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Synthetic Communications:
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Stereoselective Syntheses
of Bridgehead Hydroxy
Compounds via Reductive
Cyclization Reactions
Promoted by Samarium
Diiodide
Yung-Son Hon a , Ling Lu a & Kuan-Po Chu a
a Institute of Chemistry, Academia Sinica ,
Nankang, Taipei, Taiwan, 11529, R. O. C.
Published online: 23 Sep 2006.
To cite this article: Yung-Son Hon , Ling Lu & Kuan-Po Chu (1991) Stereoselective
Syntheses of Bridgehead Hydroxy Compounds via Reductive Cyclization Reactions
Promoted by Samarium Diiodide, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 21:18-19,
1981-1988, DOI: 10.1080/00397919108021791
To link to this article: http://dx.doi.org/10.1080/00397919108021791
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