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, 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, 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, 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, 1994; 13(1): 13-24. doi: 10.30492/ijcce.1994.10387