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Synthesis of rigid polycyclic secondary diamines: Bis-(2,3 : 6,7-iminodimethylene)anthracene and bis-(2,3 : 6,7-iminodimethylene)-9,10-dicarboxyethenoanthracene

机译:刚性多环仲二胺的合成:双-(2,3:6,7-亚氨基二亚甲基)蒽和双-(2,3:6,7-亚氨基二亚甲基)-9,10-二羧基乙炔基蒽

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摘要

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. [References: 15]
机译:通过Diels-Alder反应合成两种刚性多环仲二胺,双-(2,3:6,7-亚氨基二亚甲基)蒽和双(2,3:6,7-亚氨基二亚甲基)-9,10-二羧基乙炔基蒽描述了在1,2,4,5-四(二溴甲基)苯和马来酰亚胺之间进行酰亚胺还原。此外,这两个环状仲二胺经N-保护的氨基酸酰化,从而提供官能化的两亲性。以及用于整合到超分子系统中的手性构件。 [参考:15]

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