Issue 16, 1980

Studies on the stereochemical course of selenium-assisted cyclisation: biogentic-type synthesis in the p-menthan series

Abstract

Acid-catalysed cyclisation of the β-hydroxy selenide (3) derived from linalyl acetate (1) afforded the trans-p-methans (4) and (5), the structures of which were confirmed by their transformation into (6), (8), (9), and (11) and by alternative synthesis of these compounds.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 762-763

Studies on the stereochemical course of selenium-assisted cyclisation: biogentic-type synthesis in the p-menthan series

T. Kametani, H. Kurobe and H. Nemoto, J. Chem. Soc., Chem. Commun., 1980, 762 DOI: 10.1039/C39800000762

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