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One- and two-electron reduction of hydroxy-1,4-naphthoquinones and hydroxy-9,10-anthraquinones

✍ Scribed by Ashnagar, Alamdar; Bruce, J.Malcolm; Dutton, P.Leslie; Prince, Roger C.


Book ID
121716668
Publisher
Elsevier Science
Year
1984
Tongue
English
Weight
609 KB
Volume
801
Category
Article
ISSN
0304-4165

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πŸ“œ SIMILAR VOLUMES


Thermochemistry of 9-hydroxy-1,4-anthraq
✍ P. JimΓ©nez; M.V. Roux; J.Z. DΓ‘valos; M.T. Molina πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 English βš– 87 KB

The standard molar energy of combustion of 9-hydroxy-1,4-anthraquinone and 9-methoxy-1,4-anthraquinone were determined with a static-bomb calorimeter. The vapour pressures of the compounds were measured at temperatures between (376.61 and 394.56) K for 9-hydroxy-1,4-anthraquinone and at temperatures

Synthesis of 1-amino- and 1-hydroxy-9,10
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2-Acetyl-1,4-naphthoquinone was treated with pyrrolidine (or morpholine) enamines, derived from cyclic and acyclic ketones, in DMF at room temperature for 24-72 h to afford 3,4-disubstituted 1-pyrrolidino(or morpholino)-9,10-anthraquinones. On the other hand, when the treatment of 2-acetyl-1,4-napht