Studies on intramolecular alkylation. I. The preparation of tricyclic intermediates for the synthesis of diterpene alkaloids
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The tricyclic dienones (14), (16), and (16) have been prepared by the Ar1-6 cyclization of a diastereomeric mixture of 7-[(2?-bromo-1?- tetrahydropyranyloxy)-ethyl]-5,6,7,8-tetrahydro-2-naphthols (11) and of 7-diazoacetyl-5,6,7,8-tetrahydro-2-naphthol (17). Intermediates (11) and (17) were prepared by standard procedures from 1,2,3,4-tetrahydro- 7-hydroxy-2-naphthoic acid.
1959 ◽
Vol 24
(11)
◽
pp. 1780-1781
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1967 ◽
Vol 25
◽
pp. 78-79
1968 ◽
Vol 26
◽
pp. 284-285
1990 ◽
Vol 48
(3)
◽
pp. 502-503
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