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
ENG
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
URI
http://hdl.handle.net/10203/65453
Appears in Collection
NE-Journal Papers(저널논문)
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