An umpolung reaction of α-iminonitriles and its application to the synthesis of aminomalononitriles

Makoto Shimizu, Yuki Furukawa, Isao Mizota, Yusong Zhu

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

An umpolung N-alkylation reaction of α-iminonitriles with Grignard reagents affords the corresponding N-alkylated α-aminonitriles in good yields. Subsequent oxidation and cyanation of the N-alkylated products proceeds effectively to give aminomalononitriles in good yields, and the presence of dichlorodimethylsilane as an additive is crucial for obtaining the optimum yield. Furthermore, an electrophilic addition reaction of the intermediate halomagnesium vinylideneamide is shown to give the alkylated and acylated products in good yields.

Original languageEnglish
Pages (from-to)152-161
Number of pages10
JournalNew Journal of Chemistry
Volume44
Issue number1
DOIs
StatePublished - 2020

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