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dc.contributor.authorSreedevi, K C G-
dc.contributor.authorThomas, A P-
dc.contributor.authorSalini, P S-
dc.contributor.authorRamakrishnan, S-
dc.contributor.authorAnju, K S-
dc.contributor.authorHoladay, M G D-
dc.contributor.authorReddy, M L P-
dc.contributor.authorSuresh, C H-
dc.contributor.authorSrinivasan, A-
dc.date.accessioned2016-07-20T09:22:30Z-
dc.date.available2016-07-20T09:22:30Z-
dc.date.issued2011-11-09-
dc.identifier.citationTetrahedron Letters, 52(45):5995–5999en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2359-
dc.description.abstractA 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.isoenen_US
dc.publisherElsevieren_US
dc.title5,5-Diaryldipyrromethanes: Syntheses and Anion Binding Propertiesen_US
dc.typeArticleen_US
Appears in Collections:2011

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