Nucleophilic amination strategy for catalytic synthesis of α-amino carbonyl compounds

Ryo Yazaki

doi:10.5059/yukigoseikyokaishi.74.732

Nucleophilic amination strategy for catalytic synthesis of α-amino carbonyl compounds

Ryo Yazaki

Chemo-Pharmaceutical Sciences

Research output: Contribution to journal › Review article › peer-review

Abstract

A nucleophilic amination strategy allows for expeditious access to various N-substituted α-amino carbonyl compounds. However, development of catalytic method remained unexplored in compared to an electrophilic amination strategy. The present review focused on the recent reports of a nucleophilic amination strategy for catalytic synthesis of α-amino carbonyl compounds.

Original language	English
Pages (from-to)	732-733
Number of pages	2
Journal	Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Volume	74
Issue number	7
DOIs	https://doi.org/10.5059/yukigoseikyokaishi.74.732
Publication status	Published - Jan 1 2016

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.5059/yukigoseikyokaishi.74.732

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abstract = "A nucleophilic amination strategy allows for expeditious access to various N-substituted α-amino carbonyl compounds. However, development of catalytic method remained unexplored in compared to an electrophilic amination strategy. The present review focused on the recent reports of a nucleophilic amination strategy for catalytic synthesis of α-amino carbonyl compounds.",

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Nucleophilic amination strategy for catalytic synthesis of α-amino carbonyl compounds

Abstract

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