Calvert Matthew B, Sperry Jonathan
School of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland, 1010, New Zealand.
Chem Commun (Camb). 2015 Apr 11;51(28):6202-5. doi: 10.1039/c5cc00380f.
Guided by a biosynthetic hypothesis, a serendipitous total synthesis of yuremamine has resulted in its structural revision from the putative pyrroloindole (1) to the flavonoidal indole (2), which was initially proposed as a biosynthetic intermediate.
在生物合成假说的指导下,对育亨胺进行的一次意外全合成导致其结构从假定的吡咯并吲哚(1)修正为黄酮类吲哚(2),而黄酮类吲哚(2)最初被提议作为生物合成中间体。