Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2359
Title: 5,5-Diaryldipyrromethanes: Syntheses and Anion Binding Properties
Authors: Sreedevi, K C G
Thomas, A P
Salini, P S
Ramakrishnan, S
Anju, K S
Holaday, M G D
Reddy, M L P
Suresh, C H
Srinivasan, A
Issue Date: 9-Nov-2011
Publisher: Elsevier
Citation: 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.
Appears in Collections:2011

Files in This Item:
File Description SizeFormat 
5,5-Diaryldipyrromethanes- Sreedevi K C G- Tetrahedron letters.pdf
  Restricted Access
702.44 kBAdobe PDFView/Open Request a copy

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.