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Zur Konformation von 2-Alkyl-3-amino- und 2-Alkyl-3-ethoxyacroleinen

✍ Scribed by Skötsch, Carlo ;Breitmayer, Eberhard


Publisher
Wiley (John Wiley & Sons)
Year
1980
Tongue
English
Weight
242 KB
Volume
113
Category
Article
ISSN
0009-2940

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✦ Synopsis


Note on the Conformation of 2‐Alkyl‐3‐amino‐ and 2‐Alkyl‐3‐ethoxyacroleins

2‐Alkyl‐3‐aminoacroleins are found by ^1^H‐ and ^13^C‐NMR to prefer the E‐configuration at 30°C in hydrogen bonding solvents. In less protic solvents, the Z‐s‐Z isomer is recognized which predominates at lower temperatures. The corresponding 3‐ethoxyacroleins only exist in the E‐configuration under these conditions as their Z‐s‐Z conformation cannot be stabilized by intramolecular hydrogen bonding.


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