Desvergnes Stéphanie, Py Sandrine, Vallée Yannick
LEDSS, UMR 5616 CNRS Institut de Chimie Moléculaire de Grenoble - FR 2607 Université Joseph Fourier, B.P. 53, 38041 Grenoble, France.
J Org Chem. 2005 Feb 18;70(4):1459-62. doi: 10.1021/jo048237r.
[reaction: see text] A concise total synthesis of (+)-hyacinthacine A(2), a polyhydroxylated pyrrolizidine alkaloid, is described using our recently discovered inversion of the C-N bond polarity in nitrones. In the key step, the diastereoselective reductive coupling of a L-xylose-derived cyclic nitrone with ethyl acrylate allowed the assembly of the bicyclic core of the target molecule, by way of a tandem formation of the C-C and C-N bonds. The method opens a novel, short, and general route for the synthesis of other pyrrolizidine alkaloids.
[反应:见正文] 本文描述了使用我们最近发现的硝酮中C-N键极性反转,对多羟基吡咯里西啶生物碱(+)-风信子碱A(2)进行简洁的全合成。在关键步骤中,L-木糖衍生的环状硝酮与丙烯酸乙酯的非对映选择性还原偶联,通过C-C键和C-N键的串联形成,实现了目标分子双环核心的构建。该方法为合成其他吡咯里西啶生物碱开辟了一条新颖、简短且通用的路线。