efficient synthesis of a range of benzosubstituted macrocyclic diamides

Authors

hashem sharghi

ahmad reza massah

khodabakhsh niknam

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%.

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Journal title:
iranian journal of chemistry and chemical engineering (ijcce)

Publisher: iranian institute of research and development in chemical industries (irdci)-acecr

ISSN 1021-9986

volume 19

issue 1 2000

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