Direct access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes

Spirocycles are traditionally difficult structures to synthesize due to the congested nature of the central atom. Here the authors show a method to synthesize quaternary carbon spirocycles in one step from 1,3-enynes and pyrazolidine-type heterocycles, both relatively unactivated structures, proceed...

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Autores principales: Long Li, Shan Wang, Pengfei Luo, Ran Wang, Zheng Wang, Xiaoguang Li, Yuhua Deng, Fangzhi Peng, Zhihui Shao
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/4d3eba8180b049f1b3931c209daf7c4b
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spelling oai:doaj.org-article:4d3eba8180b049f1b3931c209daf7c4b2021-12-02T17:18:32ZDirect access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes10.1038/s41467-021-25981-x2041-1723https://doaj.org/article/4d3eba8180b049f1b3931c209daf7c4b2021-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-25981-xhttps://doaj.org/toc/2041-1723Spirocycles are traditionally difficult structures to synthesize due to the congested nature of the central atom. Here the authors show a method to synthesize quaternary carbon spirocycles in one step from 1,3-enynes and pyrazolidine-type heterocycles, both relatively unactivated structures, proceeding via palladium catalysis.Long LiShan WangPengfei LuoRan WangZheng WangXiaoguang LiYuhua DengFangzhi PengZhihui ShaoNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Long Li
Shan Wang
Pengfei Luo
Ran Wang
Zheng Wang
Xiaoguang Li
Yuhua Deng
Fangzhi Peng
Zhihui Shao
Direct access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes
description Spirocycles are traditionally difficult structures to synthesize due to the congested nature of the central atom. Here the authors show a method to synthesize quaternary carbon spirocycles in one step from 1,3-enynes and pyrazolidine-type heterocycles, both relatively unactivated structures, proceeding via palladium catalysis.
format article
author Long Li
Shan Wang
Pengfei Luo
Ran Wang
Zheng Wang
Xiaoguang Li
Yuhua Deng
Fangzhi Peng
Zhihui Shao
author_facet Long Li
Shan Wang
Pengfei Luo
Ran Wang
Zheng Wang
Xiaoguang Li
Yuhua Deng
Fangzhi Peng
Zhihui Shao
author_sort Long Li
title Direct access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes
title_short Direct access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes
title_full Direct access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes
title_fullStr Direct access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes
title_full_unstemmed Direct access to spirocycles by Pd/WingPhos-catalyzed enantioselective cycloaddition of 1,3-enynes
title_sort direct access to spirocycles by pd/wingphos-catalyzed enantioselective cycloaddition of 1,3-enynes
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/4d3eba8180b049f1b3931c209daf7c4b
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