Rao Nagavaram Narsimha, Parida Bibhuti Bhusan, Cha Jin Kun
Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States.
Org Lett. 2014 Dec 5;16(23):6208-11. doi: 10.1021/ol503136s. Epub 2014 Nov 25.
A new synthetic method for indolizidine or pyrrolizidine alkaloids based on readily available and attractively functionalized cyclopropanols, as exemplified in concise syntheses of indolizidine (-)-223AB, its 3-epimer, (-)-indolizidine 239AB, and (-)-indolizidine 239CD, is reported. This work highlights the applications of SN2' alkylation and C-acylation of cyclopropanols to meet stereochemical challenges in natural product synthesis. Also included is diastereoselective cyclization of the resulting aminoallene adduct for bicyclic ring formation.
报道了一种基于易于获得且具有吸引力的官能化环丙醇的吲哚里西啶或吡咯里西啶生物碱的新合成方法,以吲哚里西啶(-)-223AB、其3-差向异构体(-)-吲哚里西啶239AB和(-)-吲哚里西啶239CD的简洁合成为例。这项工作突出了环丙醇的SN2'烷基化和C-酰化在满足天然产物合成中的立体化学挑战方面的应用。还包括所得氨基丙二烯加合物的非对映选择性环化以形成双环。