Direct nucleophilic aromatic substitution reactions in the syntheses of anthraquinone derivatives: Chemistry and binding of podands, crown ethers, and a cryptand-Reference-Cited by-同舟云学术

Direct nucleophilic aromatic substitution reactions in the syntheses of anthraquinone derivatives: Chemistry and binding of podands, crown ethers, and a cryptand

Published:1992-08 Issue:8 Volume:5 Page:482-495
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Kim Hyunsook,Schall Otto F.,Fang Junping,Trafton John E.,Lu Tianbao,Atwood Jerry L.,Gokel George W.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference36 articles.

1. and J. Chem. Soc., Chem. Commun. 220 (1986).

2. (a) Tetrahedron Lett. 3487 (1986);

3. Electrochemical switching in anthraquinone-substituted carbon-pivot lariat ethers and podands: chain length effects in geometric and electronic cooperativity

4. Contrasting one- and two-cation binding behavior in syn- and anti-anthraquinone bibracchial podand (BiP) mono- and dianions assessed by cyclic voltammetry and electron paramagnetic resonance spectroscopy

5. Unusual 1:2 ligand:metal complex formation between an anthraquinone cryptand and lithium(+)

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