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Synlett 2015; 26(07): 965-969
DOI: 10.1055/s-0034-1380399
DOI: 10.1055/s-0034-1380399
letter
Stereocontrolled Synthesis of ABC Tricycle of Solanoeclepin A
Further Information
Publication History
Received: 04 December 2014
Accepted after revision: 22 January 2015
Publication Date:
03 March 2015 (online)
Dedicated to Professor Minoru Isobe on the occasion of his 70th birthday
Abstract
A tricyclic compound possessing oxabicyclo[2.2.1]heptane and seven-membered ring of solanoeclepin A, the most active hatching agent of potato cyst nematode, was synthesized from d-pantolactone. The synthesis features a tin-mediated 6-exo-trig radical cyclization followed by iodoetherification and ring-closing enyne metathesis.
Key words
solanoeclepin A - natural products - radical cyclization - iodoetherification - enyne metathesisSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1380399.
- Supporting Information
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References and Notes
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For recent reviews on enyne metathesis, see:
For reviews on radical conjugate additions, see:
For preparation of aluminum acetylide, see:
For the related reactions of aluminum acetylide to aldehyde, see:
Similar results were reported, see: