Literature DB >> 16292859

Rhombimines-cyclic tetraimines of trans-1,2-diaminocyclohexane shaped by the diaryl ether structural motif.

Jacek Gawroński1, Małgorzata Brzostowska, Marcin Kwit, Agnieszka Plutecka, Urszula Rychlewska.   

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.

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Year:  2005        PMID: 16292859     DOI: 10.1021/jo051687e

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

Review 1.  Imine- and Amine-Type Macrocycles Derived from Chiral Diamines and Aromatic Dialdehydes.

Authors:  Jerzy Lisowski
Journal:  Molecules       Date:  2022-06-25       Impact factor: 4.927

  1 in total

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