Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions

Asymmetric isocyanide-based multicomponent reactions are elegant, yet challenging, strategies to access valuable N-heterocycles. Here, the authors employ a chiral Mg(II) -N,N′-dioxide catalyst in three- or four-component reactions to obtain chiral tetrazoles and devise a dearomative [3+2] annulation...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Qian Xiong, Shunxi Dong, Yushuang Chen, Xiaohua Liu, Xiaoming Feng
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2019
Materias:
Q
Acceso en línea:https://doaj.org/article/acf4f00c9b424b08a7574e6fbe6e3a44
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:acf4f00c9b424b08a7574e6fbe6e3a44
record_format dspace
spelling oai:doaj.org-article:acf4f00c9b424b08a7574e6fbe6e3a442021-12-02T14:39:36ZAsymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions10.1038/s41467-019-09904-52041-1723https://doaj.org/article/acf4f00c9b424b08a7574e6fbe6e3a442019-05-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-09904-5https://doaj.org/toc/2041-1723Asymmetric isocyanide-based multicomponent reactions are elegant, yet challenging, strategies to access valuable N-heterocycles. Here, the authors employ a chiral Mg(II) -N,N′-dioxide catalyst in three- or four-component reactions to obtain chiral tetrazoles and devise a dearomative [3+2] annulation reaction of isoquinolines.Qian XiongShunxi DongYushuang ChenXiaohua LiuXiaoming FengNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Qian Xiong
Shunxi Dong
Yushuang Chen
Xiaohua Liu
Xiaoming Feng
Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
description Asymmetric isocyanide-based multicomponent reactions are elegant, yet challenging, strategies to access valuable N-heterocycles. Here, the authors employ a chiral Mg(II) -N,N′-dioxide catalyst in three- or four-component reactions to obtain chiral tetrazoles and devise a dearomative [3+2] annulation reaction of isoquinolines.
format article
author Qian Xiong
Shunxi Dong
Yushuang Chen
Xiaohua Liu
Xiaoming Feng
author_facet Qian Xiong
Shunxi Dong
Yushuang Chen
Xiaohua Liu
Xiaoming Feng
author_sort Qian Xiong
title Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
title_short Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
title_full Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
title_fullStr Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
title_full_unstemmed Asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
title_sort asymmetric synthesis of tetrazole and dihydroisoquinoline derivatives by isocyanide-based multicomponent reactions
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/acf4f00c9b424b08a7574e6fbe6e3a44
work_keys_str_mv AT qianxiong asymmetricsynthesisoftetrazoleanddihydroisoquinolinederivativesbyisocyanidebasedmulticomponentreactions
AT shunxidong asymmetricsynthesisoftetrazoleanddihydroisoquinolinederivativesbyisocyanidebasedmulticomponentreactions
AT yushuangchen asymmetricsynthesisoftetrazoleanddihydroisoquinolinederivativesbyisocyanidebasedmulticomponentreactions
AT xiaohualiu asymmetricsynthesisoftetrazoleanddihydroisoquinolinederivativesbyisocyanidebasedmulticomponentreactions
AT xiaomingfeng asymmetricsynthesisoftetrazoleanddihydroisoquinolinederivativesbyisocyanidebasedmulticomponentreactions
_version_ 1718390553301745664