Department of Chemistry, Shiraz University, Zip code 71454, Shiraz, I.R. IRAN
10.30492/ijcce.2000.10199
Abstract
Some new macrocyclic dibenzotetraoxadiamides, tribenzotetraoxadimides, tribenzopentaoxadiamide, tribenzohexaoxadiamide, and tetrabenzoheptaoxadiamide 15-22 have been prepared. These compounds were obtained in the macrocyclization step by reacting the diamines 6 and 7 with appropriate dicarboxylic acid dichlorides 8-14. The cyclization does not require high dilution techniques or template effect and provides the expected dilactams in high yields ranging from 63% to 81%.
Sharghi, H., Massah, A. R., & Niknam, K. (2000). Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides. Iranian Journal of Chemistry and Chemical Engineering, 19(1), 6-12. doi: 10.30492/ijcce.2000.10199
MLA
Hashem Sharghi; Ahmad Reza Massah; Khodabakhsh Niknam. "Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides". Iranian Journal of Chemistry and Chemical Engineering, 19, 1, 2000, 6-12. doi: 10.30492/ijcce.2000.10199
HARVARD
Sharghi, H., Massah, A. R., Niknam, K. (2000). 'Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides', Iranian Journal of Chemistry and Chemical Engineering, 19(1), pp. 6-12. doi: 10.30492/ijcce.2000.10199
VANCOUVER
Sharghi, H., Massah, A. R., Niknam, K. Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides. Iranian Journal of Chemistry and Chemical Engineering, 2000; 19(1): 6-12. doi: 10.30492/ijcce.2000.10199
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