Posada Laura, Davyt Danilo, Serra Gloria
Química Farmacéutica, Departamento de Química Orgánica, Facultad de Química, Universidad de la República General Flores 2124 CC1157 Montevideo Uruguay
Graduate Program in Chemistry, Facultad de Química, Universidad de la República Uruguay.
RSC Adv. 2020 Dec 9;10(71):43653-43659. doi: 10.1039/d0ra09635k. eCollection 2020 Nov 27.
The syntheses of versicotides A-C, natural products containing anthranilic acid and NMe-Ala, were achieved by solid phase peptide synthesis on 2-chlorotrityl resin followed by solution phase macrocyclization. Using an oxyma additive, the difficult coupling reactions to the deactivated aromatic amine of -aminobenzoic acid, were performed in high yield, avoiding anthranilic rearrangements or side reactions.
通过在2-氯三苯甲基树脂上进行固相肽合成,随后进行溶液相大环化,实现了含有邻氨基苯甲酸和N-甲基丙氨酸的天然产物versicotides A-C的合成。使用氧化膦添加剂,以高收率进行了与邻氨基苯甲酸的钝化芳香胺的困难偶联反应,避免了邻氨基苯甲酸重排或副反应。