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Dithioester
ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
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| Dithioester |
|---|
| DithiocarbonsΓ€ureester |
| R 1 , R 2 = Organylgruppe , z. B. Alkylgruppe oder Arylgruppe . Die funktionelle Gruppe ist blau markiert. |
Dithioester (DithiocarbonsΓ€ureester) bilden eine Stoffgruppe in der organischen Chemie, in der die beiden Sauerstoffatome eines CarbonsΓ€ureesters durch Schwefelatome ersetzt sind.
Contents
β’ ReaktivitΓ€t
β’ Einzelnachweise
ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
ReaktivitΓ€t
Einzelnachweise
cite-note-march-11. β Michael B. Smith: March's advanced organic chemistry, John Wiley & Sons, 7. Auflage, 2013, S. 1132β1133, ISBN 978-0-470-46259-1.