Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5284118 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
The stereoselective total synthesis of (+)-(Z)-laureatin is described. The 3,8-dioxabicyclo[5.1.1]nonane skeleton possessing trans-orientated alkyl substituents at the α,αâ²-positions to the ether linkage was stereoselectively constructed via formation of the oxetane arising from 4-exo cyclization of hydroxy epoxide existing on the oxocene core.
Keywords
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Masashi Sugimoto, Toshio Suzuki, Hisahiro Hagiwara, Takashi Hoshi,