Title of article :
Synthesis and topology of [2+2] calix[4]resorcarene-based chiral cavitand-salen macrocycles
Author/Authors :
Pappalardo، نويسنده , , Andrea and Amato، نويسنده , , Maria E. and Ballistreri، نويسنده , , Francesco P. and Notti، نويسنده , , Anna and Tomaselli، نويسنده , , Gaetano A. and Toscano، نويسنده , , Rosa M. and Sfrazzetto، نويسنده , , Giuseppe Trusso، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2012
Pages :
4
From page :
7150
To page :
7153
Abstract :
Chiral diastereomeric cavitand-salen macrocycles have been synthesized by the high-dilution condensation of a tris-(quinoxaline-bridged)-diformyl-calix[4]resorcarene with (1R,2R)-diphenylethylenediamine. The reaction produced a couple of diastereoisomers, consisting of two cavitand cavities bis-bridged by two chiral diimino moieties, which differ in a convergent (C-shaped) or divergent (S-shaped) orientation of the two cavities.
Keywords :
Diastereomeric macrocycles , tautomerism , Supramolecular chemistry
Journal title :
Tetrahedron Letters
Serial Year :
2012
Journal title :
Tetrahedron Letters
Record number :
1883209
Link To Document :
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