a convenient synthesis of macrocyclic diamides

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abstract

some new macrocyclic dibenzotrioxadiamides, dibenzotetraoxadiamide, dibenzopentaoxadiamide, dibenzothiatrioxadiamide, tribenzotrioxadiamides and tetrabenzohexaoxadiamide (14-21), (26) and (27) have been prepared. these compounds were obtained in the macrocyclization step by reacting the diamine (4) with appropriak dicaxboxylic acid dichlorides (5-13) and (24). the cyclization does not require high dilution techniques or template effect and provides the expected dilactams in high yields ranging from 70% to 95%.

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Journal title:
journal of sciences islamic republic of iran

جلد ۹، شماره ۳، صفحات ۰-۰

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