AMINO ACIDS: III. CYCLIC GUANIDINO ACIDS AND THEIR DERIVATIVES

Several new cyclic guanidino acids have been prepared by the reaction of cyclic isothioureas with amino acids. The ethyl esters of some of these acids have been converted into dialkylaminoalkylamides by refluxing with dialkylaminoalkylamines in the presence of an inert solvent. A series of dialkylam...

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Bibliographic Details
Published in:Canadian journal of chemistry 1956-06, Vol.34 (6), p.743-748
Main Authors: Garmaise, D. L, Winthrop, S. O, Grant, Gordon A, McKay, A. F
Format: Article
Language:English
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Summary:Several new cyclic guanidino acids have been prepared by the reaction of cyclic isothioureas with amino acids. The ethyl esters of some of these acids have been converted into dialkylaminoalkylamides by refluxing with dialkylaminoalkylamines in the presence of an inert solvent. A series of dialkylaminoethyl esters of the 2 -(carboxyalkylamino)- 2 -imidazolines also have been prepared.
ISSN:0008-4042
1480-3291
DOI:10.1139/v56-097