Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis
The Strecker reaction is a power method for the synthesis of cyano-substituted compounds. Here the authors report a dual-reagent system for asymmetric Strecker reactions, where an in situformed organocatalyst/methyl acrylate zwitterionic adduct activates both the cyanide source and the electrophile.
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Nature Portfolio
2016
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oai:doaj.org-article:6f18c64ef0bd4553bc9b8c7431accbb92021-12-02T17:32:50ZAsymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis10.1038/ncomms127202041-1723https://doaj.org/article/6f18c64ef0bd4553bc9b8c7431accbb92016-09-01T00:00:00Zhttps://doi.org/10.1038/ncomms12720https://doaj.org/toc/2041-1723The Strecker reaction is a power method for the synthesis of cyano-substituted compounds. Here the authors report a dual-reagent system for asymmetric Strecker reactions, where an in situformed organocatalyst/methyl acrylate zwitterionic adduct activates both the cyanide source and the electrophile.Hong-Yu WangChang-Wu ZhengZhuo ChaiJia-Xing ZhangGang ZhaoNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-9 (2016) |
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Science Q Hong-Yu Wang Chang-Wu Zheng Zhuo Chai Jia-Xing Zhang Gang Zhao Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis |
description |
The Strecker reaction is a power method for the synthesis of cyano-substituted compounds. Here the authors report a dual-reagent system for asymmetric Strecker reactions, where an in situformed organocatalyst/methyl acrylate zwitterionic adduct activates both the cyanide source and the electrophile. |
format |
article |
author |
Hong-Yu Wang Chang-Wu Zheng Zhuo Chai Jia-Xing Zhang Gang Zhao |
author_facet |
Hong-Yu Wang Chang-Wu Zheng Zhuo Chai Jia-Xing Zhang Gang Zhao |
author_sort |
Hong-Yu Wang |
title |
Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis |
title_short |
Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis |
title_full |
Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis |
title_fullStr |
Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis |
title_full_unstemmed |
Asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis |
title_sort |
asymmetric cyanation of imines via dipeptide-derived organophosphine dual-reagent catalysis |
publisher |
Nature Portfolio |
publishDate |
2016 |
url |
https://doaj.org/article/6f18c64ef0bd4553bc9b8c7431accbb9 |
work_keys_str_mv |
AT hongyuwang asymmetriccyanationofiminesviadipeptidederivedorganophosphinedualreagentcatalysis AT changwuzheng asymmetriccyanationofiminesviadipeptidederivedorganophosphinedualreagentcatalysis AT zhuochai asymmetriccyanationofiminesviadipeptidederivedorganophosphinedualreagentcatalysis AT jiaxingzhang asymmetriccyanationofiminesviadipeptidederivedorganophosphinedualreagentcatalysis AT gangzhao asymmetriccyanationofiminesviadipeptidederivedorganophosphinedualreagentcatalysis |
_version_ |
1718380194291515392 |