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Synthesis of 1,3,4-Oxadiazolidines by 1,3-Dipolar Addition of Azomethine Imines to Carbonyl Compounds

✍ Scribed by Dr. R. Grashey; cand. chem. K. Adelsberger


Publisher
John Wiley and Sons
Year
1962
Tongue
English
Weight
203 KB
Volume
1
Category
Article
ISSN
0044-8249

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✦ Synopsis


With longer-chain carbonamides, partial isomerization occurs. For example, crotonamide yields 68 % a-methylsuccinimide and 19 % glutarimide. Alicyclic unsaturated carbonamides form bicyclic imides. 0 II Cyclohexenecarbonamide forms hexahydrophthalimide in 91 % yield.


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Iminiodifluoromethanides generated by the reaction of di-undergo regioselective 1,3-dipolar cycloaddition to aldehydes to give oxazolidine derivatives. fluorocarbene with benzaldehyde and benzophenone imines