Concepedia

RhombiminesCyclic Tetraimines of <i>trans</i>-1,2-Diaminocyclohexane Shaped by the Diaryl Ether Structural Motif

Jacek Gawroński, Małgorzata Brzostowska, Marcin Kwit, A. Plutecka, Urszula Rychłewska

The Journal of Organic Chemistry · 2005 · 36 citations · 17 references

DOI

Concepts

Abstract

[reaction: see text] Rhombimines, chiral macrocyclic tetraimines, are preferentially formed because of the structural bias in the reaction of aromatic ether-linked dialdehydes with enantiomerically pure trans-1,2-diaminocyclohexane.

References

17

Shape-Persistent, Nano-Sized Macrocycles

Christian Grave, A. Dieter Schlüter · European Journal of Organic Chemistry · 2002 · 289 citations

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Ion‐Induced Tubular Assembly of Conjugated Schiff‐Base Macrocycles

A.J. Gallant, Mark J. MacLachlan · Angewandte Chemie International Edition · 2003 · 189 citations

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Designing Large Triangular Chiral Macrocycles:  Efficient [3 + 3] Diamine−Dialdehyde Condensations Based on Conformational Bias

Jacek Gawroński, Halina Kołbon, Marcin Kwit et al. · The Journal of Organic Chemistry · 2000 · 171 citations

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Synthesis and crystal structure of a novel triangular macrocyclic molecule, tris(H 2 saloph), † †H2saloph=N,N′-disalicylidene-o-phenylenediamine. and its water complex

Shigehisa Akine, Takanori Taniguchi, Tatsuya Nabeshima · Tetrahedron Letters · 2001 · 142 citations

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The synthesis of trianglimines: on the scope and limitations of the [3 + 3] cyclocondensation reaction between (1R,2R)-diaminocyclohexane and aromatic dicarboxaldehydes

Nikolai Kuhnert, Giulia M. Rossignolo, Ana M. López‐Periago · Organic & Biomolecular Chemistry · 2003 · 110 citations

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