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Synthesis 1979; 1979(4): 241-264
DOI: 10.1055/s-1979-28636
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3-Chloro-2-propeniminium-salze (vinyloge Amidchloride) als vorteilhafte Synthesebausteine der organischen Chemie

Jürgen Liebscher* , Horst Hartmann
  • *Sektion Chemie der Technischen Universität Dresden, Mommsenstr., DDR-8027 Dresden
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Publication Date:
14 May 2002 (online)

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The easily available 3-chloropropeniminium salts have recently attained synthetic importance as versatile synthons. As 1,3-bifunctional electrophilic systems, they react easily with different nucleophilic reagents to form numerous acylic and, in particular, heterocyclic compounds. 1. Synthesen von 3-Chloro-propeniminium-salzen 2. Reaktionen der 3-Chloro-2-propeniminium-salze 2.1. Reaktionen mit nucleophilen Sauerstoff-Verbindungen 2.2. Reaktionen mit nucleophilen Schwefel- bzw. Selen-Verbindungen 2.3. Reaktionen mit Aminen 2.4. Reaktionen mit nucleophilen Kohlenstoff-Verbindungen 2.5. Reaktionen mit bifunktionellen Nucleophilen 2.5.1. Synthesen von 5-Ring-Heterocyclen 2.5.2. Synthesen von 6-Ring-Heterocyclen 2.5.3. Synthesen von 7-Ring-Heterocyclen

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