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ChemInform Abstract: 5-Aminothiazolium Salts as Potential Cyclic Azomethine Ylides — Base-Induced Intramolecular Cycloaddition Reactions of N-(o-Allylphenyl)- and N-(o-(Allyloxy)phenyl)-Substituted Derivatives.

✍ Scribed by G. MOREL; E. MARCHAND; A. TOUIMI BENJELLOUN; S. SINBANDHIT; O. GUILLOU; P. GALL

Publisher: John Wiley and Sons
Year: 2010
Weight: 37 KB
Volume: 30
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199911139

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5-Aminothiazolium Salts as Potential Cyc

5-Aminothiazolium Salts as Potential Cyclic Azomethine Ylides – Base-Induced Intramolecular Cycloaddition Reactions of N-(o-Allylphenyl)- and N-(o-(Allyloxy)phenyl)-Substituted Derivatives

✍ Georges Morel; Evelyne Marchand; Adile Touimi Benjelloun; Sourisak Sinbandhit; O 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 334 KB

A series of 5-aminothiazolium chlorides (1) bearing tethered cycloadducts are deduced from their spectroscopic NMR properties and unequivocally established by an X-ray benzene ring on N-3, C-4 or the exocyclic nitrogen atom are prepared by a three-component methodology and subjected diffraction anal

ChemInform Abstract: 5-Aminothiazolium S

ChemInform Abstract: 5-Aminothiazolium Salts as Potential Cyclic Azomethine Ylides: Base-Induced Cycloaddition Reactions with Aryl, Alkyl, and Benzoyl Isothiocyanates.

✍ Adile Touimi Benjelloun; Georges Morel; Evelyne Marchand 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB