| Redox-Neutral α-Cyanation of Amines. | |
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MedLine Citation:
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PMID: 22963652 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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α-Aminonitriles inaccessible by traditional Strecker chemistry are obtained in redox-neutral fashion by direct amine α-cyanation/N-alkylation or alternatively, α-amino nitrile isomerization. These unprecedented transformations are cata-lyzed by simple carboxylic acids. |
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Authors:
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Longle Ma; Weijie Chen; Daniel Seidel |
Publication Detail:
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Type: JOURNAL ARTICLE Date: 2012-9-10 |
Journal Detail:
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Title: Journal of the American Chemical Society Volume: - ISSN: 1520-5126 ISO Abbreviation: J. Am. Chem. Soc. Publication Date: 2012 Sep |
Date Detail:
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Created Date: 2012-9-11 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 7503056 Medline TA: J Am Chem Soc Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Export Citation:
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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