Srinivasulu Chinthaginjala, Sagar Nagamangala R, Vishwanatha Thimmalapura M, Durgamma Suram, Sureshbabu Vommina V
Peptide Research Laboratory, Department of Chemistry, Jnana Bharathi, Bangalore University, Bengaluru 560056, India.
ACS Omega. 2021 Feb 10;6(7):4680-4686. doi: 10.1021/acsomega.0c05419. eCollection 2021 Feb 23.
Chiral amino acid-derived formamides represent one of the most versatile components in multicomponent reactions. Herein, we describe a facile synthesis of N-protected amino sulfenyl methyl formamides and sulfonyl methyl formamides the Mannich reaction of N-protected amino alkyl thiols followed by oxidation using 3-chloroperbenzoic acid (-CPBA). This protocol is applicable to a wide range of Fmoc- and Cbz-protected amino acids. Notably, the reaction provides high yield and retains the stereochemistry of the chiral center of the starting component.
手性氨基酸衍生的甲酰胺是多组分反应中用途最广泛的成分之一。在此,我们描述了一种简便的合成方法,通过N-保护的氨基烷基硫醇的曼尼希反应,然后用间氯过氧苯甲酸(m-CPBA)氧化,来制备N-保护的氨基亚磺酰基甲基甲酰胺和磺酰基甲基甲酰胺。该方法适用于多种Fmoc和Cbz保护的氨基酸。值得注意的是,该反应产率高,并且保留了起始组分手性中心的立体化学。