An expedient synthesis and conformational features of acylhydrazone macrocycles derived from tartaric acid: evidence of water and π aromatic hydrogen bond interactions-Reference-Cited by-同舟云学术

An expedient synthesis and conformational features of acylhydrazone macrocycles derived from tartaric acid: evidence of water and π aromatic hydrogen bond interactions

Published:2012-02 Issue:3-4 Volume:23 Page:300-305
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Skowronek Paweł,Kuncewicz Monika,Brzostowska Małgorzata,Janiak Agnieszka,Rychlewska Urszula,Gawroński Jacek

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference30 articles.

1. Tartaric and Malic Acids In Synthesis—A Source Book of Building Blocks, Ligands, Auxiliaries and Resolving Agents;Gawronski,1999

2. Molecular Receptors. Functionalized and chiral macrocyclic polyethers derived from tartaric acid

3. Factors Affecting Conformation of ( R,R )-Tartaric Acid Ester, Amide and Nitrile Derivatives. X-Ray Diffraction, Circular Dichroism, Nuclear Magnetic Resonance and Ab Initio Studies

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

5. (3+3)-Cyclocondensation of the enantiopure and racemic forms of trans-1,2-diaminocyclohexane with terephthaldehyde. Formation of diastereomeric molecular triangles and their stereoselective solid-state stacking into microporous chiral columns

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1. Synthesis of novel chiral bis-N-substituted-hydrazinecarboxamide receptors and probing their solution-phase recognition to chiral carboxylic guests by ESI-TOF/MS and tandem ESI-MS;Tetrahedron;2013-12

2. Synthesis of novel chiral tetra-(hydrazinecarboxamide) cyclophane macrocycles;Tetrahedron Letters;2013-08