The Chemistry of Laurenene. XIII. Formation of a New, Bridged, Tetracyclic Ring System
Attempted reduction of a laurenene-derived keto ester with sodium borohydride or lithium tri-t-butoxyaluminium hydride at 110° gave rise to products containing a new tetracyclic carbon ring system made up of one seven- and one six- membered ring and two five- membered rings.
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1983 ◽
Vol 241
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pp. 281-287
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1988 ◽
Vol 43
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pp. 959-962
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1992 ◽
Vol 47
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pp. 171-174
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2002 ◽
Vol 43
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pp. 4861-4864
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