Adamantane-2,4-bis(p-quinone methide) and -2,6-bis(p-quinone methide) as New Models for Intramolecular Interactions between Spatially Separated Redox Systems-Reference-Cited by-同舟云学术

Adamantane-2,4-bis(p-quinone methide) and -2,6-bis(p-quinone methide) as New Models for Intramolecular Interactions between Spatially Separated Redox Systems

Published:2001-07 Issue:7 Volume:74 Page:1327-1332
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kurata Hiroyuki,Shimoyama Takushi,Matsumoto Kouzou,Kawase Takeshi,Oda Masaji

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference19 articles.

1. Multistep reversible redox systems. 48. 1,3-Bisquinone methide cyclobutanes and related bicyclo[1.1.0]butanes: syntheses and redox properties

2. Carbon-13 nuclear magnetic resonance spectra. I—Monosubstituted adamantanes and adamantanones

3. Carbon-13 nuclear magnetic resonance spectra: V—substituent interactions at 4-substituted adamantanones and bicyclo[2.2.2]octanones

4. 13C nuclear magnetic resonance spectra—VII

5. Substituent effects on carbon-13 chemical shifts in 2,6-disubstituted adamantanes

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1. Synthesis, Structure, and Properties of Quinone Methides Incorporating Thiophene and Bithiophene Derivatives: New Overcrowded Extended Quinonoid π-Systems;Synlett;2016-06-22

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3. Photochemical Formation and Chemistry of Long-Lived Adamantylidene-Quinone Methides and 2-Adamantyl Cations;The Journal of Organic Chemistry;2009-12-03

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5. 7,7-Dipyridyl-2,6-di-tert-butyl-p-quinone Methides: Synthesis, Complexation with Silver(I) Ion, and Oxidation to Their PyridineN-Oxide;Chemistry Letters;2006-01