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2H-1,4-Thiazin-3(4H)-one durch intramolekulare anti-Michael- Addition

✍ Scribed by Wolf-Dieter Rudorf; Ralf Schwarz

Publisher: Wiley (John Wiley & Sons)
Year: 2010
Weight: 215 KB
Volume: 28
Category: Article
ISSN: 0044-2402
DOI: 10.1002/zfch.19880280204

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✦ Synopsis

S d e ) , DDR-4060 Intramolekularc Additionen von Schwefelnucleophilen an C, C-Doppel-oder C, C-Dreifachbindungen fuhren auf einfachem Wege zu Hetelocyclen [l-31. Acetylenische Carbonstiureamide des Typs 1 -leiclit zuganglich in analoger Arbeitsweise zu [4] durch Rrnktion von PhenylpropioIsaurechIorid mit N-Phcnyl-glycinestern lassen sich rnit Arylisothiocyanaten im basischen System 4 b -

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