ChemInform Abstract: A Homologation of Aldehydes and Ketones via the Formation and the Subsequent Pummerer‐Type Ring Fission of 2‐Methylsulfinyl‐5,6‐dihydro‐ 4H‐1,3,4‐thiadiazine Derivatives.

DOI DOI PDF 参考文献14件
  • Otaki Akihiro
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Shimada Kazuaki
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Yamakado Naoya
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Yanakawa Masaki
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Kagawa Takashi
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Mabuchi Shosuke
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Shimoguchi Takeshi
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Shoji Kazutoshi
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Inoue Kazuya
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University
  • Takikawa Yuji
    Department of Applied Chemistry and Molecular Science, Faculty of Engineering, Iwate University

書誌事項

タイトル別名
  • A Homologation of Aldehydes and Ketones <I>via</I> the Formation and the Subsequent Pummerer-type Ring Fission of 2-Methylsulfinyl-5,6-dihydro-<I>4H</I>-1,3,4-thiadiazine Derivatives
公開日
1995
DOI
  • 10.1246/cl.1995.925
  • 10.1002/chin.199611084
公開者
公益社団法人 日本化学会

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説明

A two-carbon homologation of aldehydes and ketones was achieved by using a sequence involving the formation and the subsequent Pummerer-type ring fission of 5,6-dihydro-4H-1,3,4-thiadiazine rings possessing methylsulfinyl functionality at C-2.

収録刊行物

  • Chemistry Letters

    Chemistry Letters 24 (10), 925-926, 1995

    公益社団法人 日本化学会

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