The clemmensen reduction of pentacyclo [
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F.J.C. Martins; L. Fourie; H.J. Venter; P.L. Wessels
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Article
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1990
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Elsevier Science
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French
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The Clenanensen reduction of pentacyclo[6.4.0.02~7.03,11.06~10], dodecane-9,12-dione unexpectedly led to the formation of pentacyclo[6.4.0. 02.6.05,9.04.12]-2-dodecanol and pentacyclo[6.4.0.02~7.03,11.06,10]dodecane-1,Gdiol as main products. Tetracyclo[6.4.0.05,9.04,12]dodecane-2,7dione and its corr