Reaction of α-iminomethylene amino esters with mono- and bidentate nucleophiles: a straightforward route to 2-amino-1H-5-imidazolones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
1. Cyclic guanidines. I. Synthesis of hypoglycemic 1-substituted 2-imino-1,3-diazacycloalkanes.
2. Cyclic guanidines. II. Synthesis of hypoglycemic acyl or alkyl derivatives of 1-substituted 2-imino-1,3-diazacycloalkane.
3. Cyclic guanidines. III. Synthesis of hypoglycemic 2-benzhydrylimino-1,3-diazacycloalkanes.
4. Cyclic guanidines. IV. Synthesis of hypoglycemic N-benzhydryl bicyclic guanidines.
5. Synthesis and biological activity of spirocyclic benzopyran imidazolone potassium channel openers
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3. Derivatives of Azidocinnamic Acid in the Synthesis of 2-Amino-4-Arylidene-1H-Imidazol-5(4H)-Ones;Chemistry of Heterocyclic Compounds;2018-06
4. Ph3P/I2-Mediated Synthesis of N,N′,N″-Substituted Guanidines and 2-Iminoimidazolin-4-ones from Aryl Isothiocyanates;The Journal of Organic Chemistry;2017-09-12
5. Molecular-Iodine-Mediated, Efficient One-Pot Synthesis of 2-Iminohydantoins and 2-Amino-1H-imidazol-4(5H)-ones by Cyclodeselenization of Selenourea-Tethered Amides/Peptides;ChemistrySelect;2017-01-23
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