Australian Journal of Chemistry

3, 4, 5, 6, 7, 8-Hexahydronaphthalen-1 (2H)-ones. Synthesis and photoaddition to (Z)-1, 2-Dichloroethylene

ID Rae, BN Umbrasas

文献索引：Rae,I.D.; Umbrasas,B.N. Australian Journal of Chemistry, 1975 , vol. 28, p. 2669 - 2680

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被引用次数: 14

摘要

Abstract Several cyclohexanones have been converted, via cyclohexylidenebutyric acids, into 3, 4, 5, 6, 7, 8-hexa-hydronaphthalen-1 (2H)-ones in good yield. Cyclododecanone gives bicyclo [10, 4, 0] hexadec-1 (12)-en-13-one. Heating 3, 4, 5, 6, 7, 8- hexahydronaphthalen-1 (2H)-one with polyphosphoric acid gives 1, 2, 3, 4- tetrahydronaphthalene, but the 7-methyl octalone gives the 2-and 6-methyl tetralins. ...