Synthesis and Tautomerism of 1,5-Bis(alkylamino)-4H-benzo[a]phenothiazin-4-ones
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/63/5/63_5_1467/_pdf
Reference26 articles.
1. Synthesis of some 5H-benzo[a]phenothiazin-5-one derivatives
2. Synthesis of 1- and 4-substituted-5H-benzo[a]phenoxazin-5-ones
3. The photochemical reactions of 5H-benzo[a]phenoxazin-5-one with alkylthiols and thiophenol
4. The reaction products of 2H-isoindole-4,7-dione derivatives with 2-aminobenzenethiol
5. The condensation products of 2,3,6-trisubstituted-1,4-naphthoquinones with 2-aminothiophenol
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2. Effect of substitutents on the tautomeric equilibrium of 5-hydroxy-1,4-naphthoquinon-4-imines;Russian Chemical Bulletin;1997-02
3. Synthesis of Indolo phenothiazin-6-one derivatives;Monatshefte f�r Chemie Chemical Monthly;1993-03
4. A Smiles Rearrangement as an Intermediate Step in the Formation of 8-Bromo-7-hydroxy-N-(4’ -N,N-diethylaminophenyl)-12H-benzo[b]phenothiazine-6,11-quinone 6-lmine from 2-(2’ -Aminophenylthio)-6-bromo-5-hydroxy-N-(4-/V,/V-diethylaminophenyl)-1,4-naphthoquinone 4-lmine;Mendeleev Communications;1993-01
5. Synthesis of Novel Polycyclic Selenepinone Compounds;Bulletin of the Chemical Society of Japan;1992-07
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