On the Extent of Transannular Rearrangement in the Formolysis of 1,5-Cyclooctadiene Monoepoxide
Formolysis of 1,5-cyclooctadiene monoepoxide (1) has been shown to give only ca. 25% of products of transannular reactions. The difference between this result and those from the solvolyses of cyclooctene oxide and 4-cyclooctenyl brosylate is attributed to conformational and ring-strain effects.
1974 ◽
Vol 39
(15)
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pp. 2276-2281
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1971 ◽
Vol 93
(8)
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pp. 1962-1967
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Keyword(s):
1997 ◽
Vol 38
(35)
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pp. 6177-6180
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Keyword(s):
1995 ◽
Vol 337
(1)
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pp. 60-62
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