Journal of the Chemical Society. Perkin transactions I p. 756 - 760 (1981)
Update date:2022-08-02
Topics:
Kametani, Tetsuji
Kurobe, Hiroshi
Nemoto, Hideo
Acid-catalysed cyclization of the β-hydroxyselenide (3), derived from linalyl acetate (1), afforded the trans-p-menthanes (4) and (5), the structures of which were confirmed by their transformation into (6), (11), (8), and (13), and alternative syntheses of these compounds.The structure determination of some products obtained by the reaction of limonene and α-terpineol epoxides with phenylselenium anion was also carried out.
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Doi:10.1007/BF00507248
(1981)Doi:10.1016/j.ejps.2006.05.010
(2006)Doi:10.1021/jm00310a047
(1968)Doi:10.1081/NCN-200060173
(2005)Doi:10.1081/NCN-200060085
(2005)Doi:10.1081/NCN-200060244
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