化学
巴非霉素
不对称诱导
立体化学
Stille反应
碳二亚胺
等结构
组合化学
对映选择合成
有机化学
晶体结构
生物化学
催化作用
细胞凋亡
自噬
作者
Stephen Hanessian,Jianguo Ma,Wengui Wang
摘要
The macrolide bafilomycin A(1) was synthesized starting from D-valine and D-mannitol as chiral progenitors of propionate units. Acyclic subunits corresponding to different parts of the molecule were constructed based on an iterative 1,2-asymmetric induction protocol as a distinctive feature of the synthesis. The assembly of two segments encompassing the entire carbon framework of the macrolide was achieved by using a Stille coupling. The resulting seco-ester was further manipulated to provide crystalline bafilomycin A(1) via a conventional carbodiimide-mediated Keck-type macrolactonization.
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