Please use this identifier to cite or link to this item: http://idr.niser.ac.in:8080/jspui/handle/123456789/932
Title: 5,5-Diaryldipyrromethanes: syntheses and anion binding properties
Authors: Srinivasan, A.
Issue Date: 9-Nov-2011
Publisher: Tetrahedron Letters
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.
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.
URI: https://doi.org/10.1016/j.tetlet.2011.08.163
http://idr.niser.ac.in:8080/jspui/handle/123456789/932
Appears in Collections:Journal Papers

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