Title of article
A three-step and enantioselective synthesis of (−)-(S)- or (+)-(R)-2-(furan-3-yl)-3,6-dihydro-2H-pyrans
Author/Authors
de Rosa، نويسنده , , Margherita and Solladié-Cavallo *، نويسنده , , Arlette and Scettri، نويسنده , , Arrigo، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
4
From page
1593
To page
1596
Abstract
Enantiomerically enriched (3-furyl)-2-pyran derivatives, key-intermediates in the synthesis of the pharmacophoric pyranofuranone system of the bioactive natural products manoalide and cacospongionolide B, are easily accessible by a rapid sequence involving a chiral allylation and a ring closing metathesis reaction.
Keywords
ring-closing metathesis , furyl-dihydropyranes , Asymmetric allylation
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1636535
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