Reaction of Bicyclic Amide Acetals with Carboxylic Acids and their Anhydrides
β Scribed by Dr. R. Feinauer
- Publisher
- John Wiley and Sons
- Year
- 1967
- Tongue
- English
- Weight
- 218 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0044-8249
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β¦ Synopsis
The reactivity of the aziridinium cation towards the hydroxyl group of alcohols and phenols makes possible a simple synthesis of 2-alkoxyethylamines 111.
If the reaction is carried out with a-hydroxy esters ( I ) and aziridinium tetrafluoroborate (2), one obtains first the salts (3) and then, by loss of alcohol, 2-substituted 3-oxapentane-5-lactams (2-morpholinones) (4) together with linear polyamides.
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Linear, soluble copolymers containing titanium are of interest for use in targets for inertial-confinement fusion (ICF) experiments because the titanium is a useful spectroscopic probe for studying the nuclear fusion process. We have studied the reactions of dichlorotitanocene and diphenyltitanocene
Acyclic secondary amides such as benzanilides 1a-g, acetanilides 2a-d, and benzamide 1h undergo selfcondensation in the presence of phosphoric anhydride to produce, in one step, N-substituted aroyl benzamidines 3a-g, acyl acetamidines 4a-d, and imide 5, respectively. Mechanistic evidence is presente