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摘要
A mild, cost-effective, and simple three-component Ugi-type reaction using p-toluenesulfinic acid (pTSIA) as the acid catalyst has been developed to synthesize alpha-amino amides and alpha-amino amidines. Employing 1 equiv of amine used in the reaction generated alpha-amino amides exclusively, while 2 equiv of amines, especially with more nucleophilic aniline such as p-anisidine, yielded the alpha-amino amidines as the major product. This methodology would be suitable for the synthesis of natural or unnatural amino acids and drug-like amidine analogues. Published by Elsevier Ltd.
- 出版日期2013-5-8
