The Reaction of Enamines with N-Dialkylchloramines

DOI DOI

この論文をさがす

説明

The reaction of dialkylchloramines with N-dialkyl-substituted aminoisobutenes was shown to give a mixture of the two α-dialkylaminoaldehydes, which were derived not only from the addition of chloramine, but also from the rearrangement of amino group in the parent enamines. The results suggested an ionic path involving _??_ cyclic dialkylaziridiniurn ion as intermediate. The possible mechanism of these reactions was discussed.

収録刊行物

キーワード

詳細情報 詳細情報について

  • CRID
    1390282681446601472
  • NII論文ID
    130003523934
  • DOI
    10.1271/bbb1961.36.799
    10.1080/00021369.1972.10860313
  • COI
    1:CAS:528:DyaE38XktlektLc%3D
  • ISSN
    18811280
    00021369
  • 本文言語コード
    en
  • データソース種別
    • JaLC
    • Crossref
    • CiNii Articles
    • OpenAIRE
  • 抄録ライセンスフラグ
    使用不可

問題の指摘

ページトップへ