Gerasyuto Aleksey I, Hsung Richard P
Division of Pharmaceutical Sciences and Department of Chemistry, Rennebohm Hall, 777 Highland Avenue, University of Wisconsin, Madison, Wisconsin 53705, USA.
Org Lett. 2006 Oct 12;8(21):4899-902. doi: 10.1021/ol0619359.
[structure: see text] A stereodivergent approach toward total syntheses of Coccinellidae defensive alkaloids is described. These syntheses feature a highly diastereoselective intramolecular aza-[3 + 3] annulation strategy, which represents a de novo approach to this family of natural products.
[结构:见正文] 描述了一种用于全合成瓢虫科防御性生物碱的立体发散方法。这些合成以高度非对映选择性的分子内氮杂-[3 + 3]环化策略为特征,这代表了一种针对此类天然产物家族的全新方法。