Volume 22, Issue 39
Heterocyclic Compounds
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ChemInform Abstract: Preparation and Structural Properties of Large-Cavity Peraza Macrocycles Containing Pyridine, Phenanthroline, or Piperazine Subcyclic Units.

K. E. KRAKOWIAK

K. E. KRAKOWIAK

Dep. Chem., Brigham Young Univ., Provo, UT 84602, USA

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J. S. BRADSHAW

J. S. BRADSHAW

Dep. Chem., Brigham Young Univ., Provo, UT 84602, USA

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W. JIANG

W. JIANG

Dep. Chem., Brigham Young Univ., Provo, UT 84602, USA

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N. K. DALLEY

N. K. DALLEY

Dep. Chem., Brigham Young Univ., Provo, UT 84602, USA

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G. WU

G. WU

Dep. Chem., Brigham Young Univ., Provo, UT 84602, USA

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R. M. IZATT

R. M. IZATT

Dep. Chem., Brigham Young Univ., Provo, UT 84602, USA

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First published: October 1, 1991

Abstract

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ChemInform Abstract

Reaction of the pyridinedicarbaldehyde (Ia) or the diacetylpyridine ( Ib) with the triamine (II) followed by reduction with sodium borohydride forms the macrocycles (III). The tetraazomethines (VI) are prepared by reaction of the phenanthrolinedicarbaldehyde (IV) with the diamines (V). Reaction of N,N′-di(chloromethylcarbonyl)piperazine (VII) with piperazine (VIII) yields the macrocycles (IX) and (X).

chemical structure image

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