**Oxidative Coupling of CH‐acid Compounds with p‐Phenylenediamines. VII. Synthesis and Oxidative Coupling of 5‐Hydroxy‐naphth[2,1‐d] 1,3‐oxathiol‐2‐ones** 5‐Hydroxy‐naphth[2,1‐d]1,3‐oxathiol‐2‐ones with different substituents **1**–**21** were synthesized using the following procedures: Condensatio
Oxidative Kupplung CH-acider Verbindungen mit p-Phenylendiaminen. V. Massenspektrometrische Fragmentierung von 4-substituierten 3-Methyl-1-phenyl-pyrazolin-5-onen
✍ Scribed by Dr. H. Wilde; Doz. Dr. R. Herzschuh; Dipl.-Chem. P. Lepom; Prof. Dr. G. Mann
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 253 KB
- Volume
- 323
- Category
- Article
- ISSN
- 1615-4150
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✦ Synopsis
Oxidative Coupling of CH‐acid Compounds with p‐Phenylenediamines. V. Mass Spectrometric Fragmentation of 4‐Substituted 3‐Methyl‐1‐phenyl‐pyrazolin‐5‐ones
The mass spectra of 3‐methyl‐1‐phenyl‐pyrazolin‐5‐one 1 and 4‐substituted derivatives 2–18 have been studied and the fragmentation mechanisms are discussed. The major cleavages take place in three ways, whose significance is related to the properties of the substituents. The mass spectra permit the determination of the structure, purity and stability of the substituted colour couplers.
📜 SIMILAR VOLUMES
**Oxidative Coupling of CH‐acid Compounds with p‐Phenylenediamines. VIII. Synthesis of 5H‐Benzo[a]phenothiazin‐5‐ones from Naphth[2,1‐d]1,3‐oxathiol‐2‐ones** Reaction of 5‐hydroxynaphth[2,1‐d]1,3‐oxathiol‐2‐ones with N,N‐diethyl‐quinone‐1,4‐diimine leads to 5H‐benzo[a]phenothiazin‐5‐ones **1**–**21