作者:Srivari Chandrasekhar、Chennamaneni Lohitha Rao、Mallikanti Seenaiah、Police Naresh、Bharatam Jagadeesh、Dharani Manjeera、Arpita Sarkar、Manika Pal Bhadra
DOI:10.1021/jo8020264
日期:2009.1.2
An efficient and practical total synthesis of marine cyclic tetrapeptide, natural product azumamide E (1) is achieved via high-yielding reactions. The strategy also allowed us to synthesize the azumamide E-SAA (sugar amino acid) analogue (2), whose solution-phase NMR and biological activity studies were also carried out.
通过高产率反应,可以有效,实用地合成海洋环四肽,天然产物氮酰胺E(1)。该策略还使我们能够合成the酰胺E-SAA(糖氨基酸)类似物(2),其溶液相NMR和生物活性研究也已进行。