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ChemInform Abstract: Halogenoarylation of Allyl Isothiocyanate: Synthesis of 2,5-Disubstituted 2-Thiazolines.

✍ Scribed by Mykola D. Obushak; Volodymyr V. Karpyak; Mykola I. Ganushchak

Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
30
Category
Article
ISSN
0931-7597

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πŸ“œ SIMILAR VOLUMES

Halogenoarylation of allyl isothiocyanat
Halogenoarylation of allyl isothiocyanate: Synthesis of 2,5-disubstituted 2-thiazolines
✍ Mykola D. Obushak; Volodymyr V. Karpyak; Mykola I. Ganushchak πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 239 KB

A new approach to the synthesis of 2-R-5-benzyl-2-thiazolines with the use of chloro-and bromoarylation products of allyl isothiocyanate with arenediazonium halides was elaborated. The isothiocyanates obtained were reacted with ammonia, aliphatic or aromatic amines, and sodium methoxide. The use of

ChemInform Abstract: Preparation of 2,5-
ChemInform Abstract: Preparation of 2,5-Disubstituted 2-Thiazolines.
✍ V. V. KARPYAK; N. D. OBUSHAK; N. I. GANUSHCHAK πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 1 views

Preparation of 2,5-Disubstituted 2-Thiazolines. -A new synthetic access to the title thiazolines is presented. The isothiocyanates (I) and (VI), prepared by chloroarylation of allylisothiocyanate with aryldiazonium chlorides, undergo cyclization in the presence of bases to afford the target thiazol

ChemInform Abstract: Diastereoselective
ChemInform Abstract: Diastereoselective Synthesis of 2,5-Disubstituted Tetrahydrofuran Derivatives.
✍ Ronaldo A. Pilli; Valeria B. Riatto πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons βš– 31 KB

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