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
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.
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.
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.
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.
', './data/ijcce/coversheet/cover_en.jpg'))