A STEREOCONTROLLED SYNTHESIS OF ANTI-2,5-DISUBSTITUTED TETRAHYDROFURANS
Anti-2,5-disubstituted tetrahydrofurans, in which one of the substituents is 3'-furanyl group, have been derived from trans-4-(3'-furanyl)-3-butenols 3-8 by using iodine in diethyl ether in the presence of potassium carbonate at -78-degrees-C.
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Issue Date
- 1993-03
- Language
- English
- Article Type
- Article
- Keywords
TRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS; ABSOLUTE-CONFIGURATION; IODOETHERIFICATION; VERRUCOSIDIN; INDUCTION; ROUTE
- Citation
TETRAHEDRON LETTERS, v.34, no.12, pp.1955 - 1958
- ISSN
- 0040-4039
- Appears in Collection
- CH-Journal Papers(저널논문)
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