N,N-Di- and N,N,C-Trialkylation of α-Sulfoximino Esters

• Hata Shingo

  Department of Chemistry for Materials, Graduate School of Engineering, Mie University

• Maeda Tatsuya

  Department of Chemistry for Materials, Graduate School of Engineering, Mie University

• Shimizu Makoto

  Department of Chemistry for Materials, Graduate School of Engineering, Mie University

書誌事項

タイトル別名

• <i>N</i>,<i>N</i>-Di- and <i>N</i>,<i>N</i>,<i>C</i>-Trialkylation of α-Sulfoximino Esters

抄録

N,N-Dialkylation of α-sulfoximino esters with Grignard reagents proceeds to give α-N,N-dialkylamino esters. N,N,C-Trialkylated product is also obtained via the oxidation and nucleophilic addition reaction of the intermediary enolate.

収録刊行物

• Bulletin of the Chemical Society of Japan

  Bulletin of the Chemical Society of Japan 85 (11), 1203-1205, 2012

  公益社団法人 日本化学会

キーワード

• General Chemistry

詳細情報

• CRID: 1390282679120081408
• NII論文ID: 130004153004
• NII論文ID: 10031126535
• NII書誌ID: AA00580132
• DOI: 10.1246/bcsj.20120195
• COI: 1:CAS:528:DC%2BC38XhslOis73J
• ISSN: 13480634
• ISSN: 00092673
• NDL書誌ID: 024075921
• Web Site: http://id.ndl.go.jp/bib/024075921
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I024075921
• Web Site: https://academic.oup.com/bcsj/article-pdf/85/11/1203/56274339/bcsj.20120195.pdf
• 本文言語コード: en
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