Novel synthesis of macrocycles with 1,1′-binaphthalene-2,2′-diol using intramolecular oxidative coupling

Author:

Ito Satoshi,Koizumi Kazuya,Fukuda Katsuhiko,Kameta Naohiro,Ikeda Tsukasa,Oba Toru,Hiratani Kazuhisa

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. In Host–Guest Complex Chemistry I, II, and III; Voegtle, F., Ed.; Springer-Verlag-VCH: Berlin, 1981 (I), 1982 (II), 1984 (III); In Inclusion Compounds vols. 1–5; Atwood, J. L.; Davies, J. E. D.; MacNicol, D. D., Eds.; Academic Press: London, 1984 (Vols. 1–3); 1991 (Vols. 4–5).

2. A widely useful chiral stationary phase for the high-performance liquid chromatography separation of enantiomers

3. Chiral HPLC (high-performance liquid chromatographic) stationary phases. 4. Separation of the enantiomers of bi-.beta. naphthols and analogs

4. Synthesis and binding characteristics of macrocyclic polyethers containing convergent methoxyaryl or phenolic groups

5. Host-guest complexation. 19. Cyclic, bicyclic, and tricyclic polyether systems

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