1
CUNY Graduate Center, Department of Chemistry, Hunter College, New York, N.Y. 10021, USA
2
Research Division, Hoffimann-La Roche, Inc., Nutly, NJ 07110, USA
10.30492/ijcce.1994.10387
Abstract
Results of the bromination and dehydrobromination of several angular methylated decalindiones are described. The key reaction, base-induced cyclization of the monobromo keto ester (3), and the dibromo ketone (4), leads to the formation of tricyclic systems (6) and (9) respectively.
Karimi, S., Grohamann, K., Todaro, L. (1994). Bromination and Dehydrobromination Studies on Some CIS-4a-Methyl-Decaline-2,7-Diones. Iranian Journal of Chemistry and Chemical Engineering (IJCCE), 13(1), 13-24. doi: 10.30492/ijcce.1994.10387
MLA
Sasanin Karimi; K. Grohamann; L. Todaro. "Bromination and Dehydrobromination Studies on Some CIS-4a-Methyl-Decaline-2,7-Diones". Iranian Journal of Chemistry and Chemical Engineering (IJCCE), 13, 1, 1994, 13-24. doi: 10.30492/ijcce.1994.10387
HARVARD
Karimi, S., Grohamann, K., Todaro, L. (1994). 'Bromination and Dehydrobromination Studies on Some CIS-4a-Methyl-Decaline-2,7-Diones', Iranian Journal of Chemistry and Chemical Engineering (IJCCE), 13(1), pp. 13-24. doi: 10.30492/ijcce.1994.10387
VANCOUVER
Karimi, S., Grohamann, K., Todaro, L. Bromination and Dehydrobromination Studies on Some CIS-4a-Methyl-Decaline-2,7-Diones. Iranian Journal of Chemistry and Chemical Engineering (IJCCE), 1994; 13(1): 13-24. doi: 10.30492/ijcce.1994.10387
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