5,5-Diaryldipyrromethanes: syntheses and anion binding properties

Please use this identifier to cite or link to this item: http://idr.niser.ac.in:8080/jspui/handle/123456789/932

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DC Field	Value	Language
dc.contributor.author	Srinivasan, A.	-
dc.date.accessioned	2024-11-20T08:53:53Z	-
dc.date.available	2024-11-20T08:53:53Z	-
dc.date.issued	2011-11-09	-
dc.identifier.citation	Gowri Sreedevi, K. C., Thomas, A. P., Salini, P. S., Ramakrishnan, S., Anju, K. S., Derry Holaday, M. G., … Srinivasan, A. (2011). 5,5-Diaryldipyrromethanes: syntheses and anion binding properties. Tetrahedron Letters, 52(45), 5995–5999.	en_US
dc.identifier.uri	https://doi.org/10.1016/j.tetlet.2011.08.163	-
dc.identifier.uri	http://idr.niser.ac.in:8080/jspui/handle/123456789/932	-
dc.description.abstract	A two-step synthesis of 5,5-diaryldipyrromethanes in good yields is described. The adopted synthetic strategy can be used to tune the substituent at the meso-carbon very easily by choosing the Grignard reagent of interest. Further, the influence of the incorporation of various diaryl units at the meso-carbon atom in the inherent anion binding affinities of the dipyrromethanes through hydrogen bonding was discussed.	en_US
dc.language.iso	en	en_US
dc.publisher	Tetrahedron Letters	en_US
dc.title	5,5-Diaryldipyrromethanes: syntheses and anion binding properties	en_US
dc.type	Article	en_US
Appears in Collections:	Journal Papers

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