Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5280679 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Chiral lactones were synthesized in six steps from d-mannitol. The key-step was a domino ring-closing metathesis reaction leading to the symmetric cleavage of a d-mannitol triene derivative and to the formation of two molecules of the desired lactone.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bastien Nay, Nicolas Gaboriaud-Kolar, Bernard Bodo,