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Synlett 2003(9): 1361-1363
DOI: 10.1055/s-2003-40359
DOI: 10.1055/s-2003-40359
LETTER
© Georg Thieme Verlag Stuttgart ˙ New York
Synthesis of Rigid Polycyclic Secondary Diamines: Bis-(2,3:6,7-Iminodimethylene)anthracene and Bis-(2,3:6,7-Iminodimethylene)-9,10-dicarboxyethenoanthracene
Further Information
Received
17 March 2003
Publication Date:
30 June 2003 (online)
Publication History
Publication Date:
30 June 2003 (online)
Abstract
The synthesis of two rigid polycyclic secondary diamines, bis-(2,3:6,7-iminodimethylene)anthracene and bis-(2,3:6,7-iminodimethylene)-9,10-dicarboxyethenoanthracene, by means of Diels-Alder reaction between 1,2,4,5-tetra(dibromomethyl)benzene and maleimides followed by imide reduction, is described. Furthermore, these two cyclic secondary diamines undergo acylation with N-protected amino acids, thus providing functionalized, amphiphilic, and chiral building blocks for incorporation into supramolecular systems.
Key words
arenes - amino acids - Diels-Alder reactions - polycycles
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