Construction of a BCDE Core of Furanosteroids Enabled by Nickel-Promoted Reductive Cyclization

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Li-Jun Xu,  and , Yu Peng*, 
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Abstract

We developed a new synthetic strategy for furanosteroids and constructed the BE ring system in one step by a Ni-catalyzed reductive cyclization cascade. The subsequent oxidative elaboration led to the efficient formation of a BCDE tetracyclic core embedded in these furanosteroids. Furthermore, a synthesis of the carbon skeleton of nodulisporiviridin C was achieved, as well, through this method.

Abstract Image

Abstract Image

镍促进还原环化的呋喃甾体BCDE核的构建
本文提出了一种新的呋喃甾体合成策略,并通过镍催化还原环化级联一步构建了BE环体系。随后的氧化精化导致嵌入在这些呋喃甾体中的BCDE四环核的有效形成。此外,还通过该方法合成了结核孢绿素C的碳骨架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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