Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers

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DC Field	Value	Language
dc.contributor.author	GADEKAR, SANTOSH C.	en_US
dc.contributor.author	REDDY, BADDIGAM K.	en_US
dc.contributor.author	PANCHAL, SANTOSH P.	en_US
dc.contributor.author	ANAND, V. G.	en_US
dc.date.accessioned	2019-04-29T10:14:36Z
dc.date.available	2019-04-29T10:14:36Z
dc.date.issued	2016-03	en_US
dc.identifier.citation	Chemical Communications, 52(24), 4565-4568.	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.issn	1364-548X	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2678	-
dc.identifier.uri	https://doi.org/10.1039/C5CC10356H	en_US
dc.description.abstract	Benzofused dipyrrins react with metal salt copper(II) acetate to predominantly yield a cyclodimer along with a cyclotrimer. N-confused monobenzo-dipyrrin cyclomerized to trioxo-expanded norrole 13a and an acyclic dimer 14 whereas doubly N-confused monobenzo and dibenzo-dipyrrins yielded aza-heptalene 15 and an acyclic dimer 16.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Cyclomerization	en_US
dc.subject	Benzodipyrrins	en_US
dc.subject	Acyclic dimers	en_US
dc.subject	Macrocyclic framework	en_US
dc.subject	2016	en_US
dc.title	Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Chemical Communications	en_US
dc.publication.originofpublisher	Foreign	en_US
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