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通过N-叔丁氧羰基-双吡啶的锂化反应简洁合成(±)-金雀花碱。

Concise synthesis of (+/-)-cytisine via lithiation of N-Boc-bispidine.

作者信息

Stead Darren, O'Brien Peter, Sanderson Adam J

机构信息

Department of Chemistry, University of York, Heslington, York YO10 5DD, UK.

出版信息

Org Lett. 2005 Sep 29;7(20):4459-62. doi: 10.1021/ol0516869.

Abstract

[reaction: see text] (+/-)-Cytisine has been synthesized in 19% overall yield via a six-step approach from commercially available materials. Key features of this new strategy are as follows: (i) initial construction of the bispidine core, (ii) lithiation-transmetalation-allylation of an N-Boc-bispidine, and (iii) a Pd/C-mediated dihydropyridone oxidation-N-debenzylation process.

摘要

[反应:见正文] (±)-金雀花碱已通过一种由市售原料出发的六步方法以19%的总收率合成。这一新策略的关键特征如下:(i)双哌啶核心的初步构建,(ii)N-叔丁氧羰基-双哌啶的锂化-金属转移-烯丙基化,以及(iii)钯/碳介导的二氢吡啶酮氧化-N-脱苄基过程。

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