Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides

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 ac...

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Main Authors:	Hashem Sharghi, Ahmad Reza Massah, Khodabakhsh Niknam
Format:	Article
Language:	English
Published:	Iranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECR 2000-06-01
Series:	Iranian Journal of Chemistry & Chemical Engineering
Subjects:	macrocyclic diamides synthesis direct macrocyclization dicarboxylic acid dichloride
Online Access:	http://www.ijcce.ac.ir/article_10199_3f0816a9e5003cff873ee9a0e8775719.pdf

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spelling	doaj-9b154698443a4fc59137707b70cfde482020-11-25T03:31:53ZengIranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECRIranian Journal of Chemistry & Chemical Engineering 1021-99861021-99862000-06-0119161210199Efficient Synthesis of a Range of Benzosubstituted Macrocyclic DiamidesHashem Sharghi0Ahmad Reza Massah1Khodabakhsh Niknam2Department of Chemistry, Shiraz University, Zip code 71454, Shiraz, I.R. IRANDepartment of Chemistry, Shiraz University, Zip code 71454, Shiraz, I.R. IRANDepartment of Chemistry, Shiraz University, Zip code 71454, Shiraz, I.R. IRANSome 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%.http://www.ijcce.ac.ir/article_10199_3f0816a9e5003cff873ee9a0e8775719.pdfmacrocyclic diamidessynthesisdirect macrocyclizationdicarboxylic acid dichloride
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Hashem Sharghi Ahmad Reza Massah Khodabakhsh Niknam
spellingShingle	Hashem Sharghi Ahmad Reza Massah Khodabakhsh Niknam Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides Iranian Journal of Chemistry & Chemical Engineering macrocyclic diamides synthesis direct macrocyclization dicarboxylic acid dichloride
author_facet	Hashem Sharghi Ahmad Reza Massah Khodabakhsh Niknam
author_sort	Hashem Sharghi
title	Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides
title_short	Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides
title_full	Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides
title_fullStr	Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides
title_full_unstemmed	Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides
title_sort	efficient synthesis of a range of benzosubstituted macrocyclic diamides
publisher	Iranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECR
series	Iranian Journal of Chemistry & Chemical Engineering
issn	1021-9986 1021-9986
publishDate	2000-06-01
description	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%.
topic	macrocyclic diamides synthesis direct macrocyclization dicarboxylic acid dichloride
url	http://www.ijcce.ac.ir/article_10199_3f0816a9e5003cff873ee9a0e8775719.pdf
work_keys_str_mv	AT hashemsharghi efficientsynthesisofarangeofbenzosubstitutedmacrocyclicdiamides AT ahmadrezamassah efficientsynthesisofarangeofbenzosubstitutedmacrocyclicdiamides AT khodabakhshniknam efficientsynthesisofarangeofbenzosubstitutedmacrocyclicdiamides
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Efficient Synthesis of a Range of Benzosubstituted Macrocyclic Diamides

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