Issue 2, 1975

Synthesis and reactions of isoprenyl terminal epoxides in the chromone and quinoline series

Abstract

The prenylchromone peucenin (9a) was converted into the terminal olefin (11) and the terminal epoxide (13); acid- and base-catalysed cyclisation of the latter furnished a pyranochromone (14a), and the pyranoquinoline (21) was prepared similarly. The furochromone (±)-visamminol (8) was synthesised from peucenin.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 150-154

Synthesis and reactions of isoprenyl terminal epoxides in the chromone and quinoline series

M. F. Grundon and H. M. Okely, J. Chem. Soc., Perkin Trans. 1, 1975, 150 DOI: 10.1039/P19750000150

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