作者:Ryan D. White、Gregg F. Keaney、Corin D. Slown、John L. Wood
DOI:10.1021/ol049918b
日期:2004.4.1
The total synthesis of kalihinol C, a bis-isonitrile marine diterpenoid isolated from Acanthella sp., is reported. The decalin framework was established via an intramolecular Diels-Alder cycloaddition and subsequently functionalized through a series of substrate-controlled diastereoselective transformations to install the tertiary isonitrile, beta-hydroxy isonitrile, and pendant tetrahydrofuranyl ring
据报道,从卡那氏菌属(Acanthella sp。)分离出的双异腈海洋二萜kalihinol C的总合成。萘烷骨架是通过分子内Diels-Alder环加成反应建立的,随后通过一系列底物控制的非对映选择性转化进行功能化,以安装叔异腈,β-羟基异腈和侧链四氢呋喃基环。