Photochemistry of 3-Amino-2-Alkenimines: Synthesis of Substituted Quinolines

  1. Campos, P.J. 1
  2. Tan, C.-Q. 1
  3. González, J.M. 2
  4. Rodríguez, M.A. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

  2. 2 Universidad de Oviedo
    info

    Universidad de Oviedo

    Oviedo, España

    ROR https://ror.org/006gksa02

Journal:
Tetrahedron Letters

ISSN: 0040-4039

Year of publication: 1993

Volume: 34

Issue: 33

Pages: 5321-5324

Type: Article

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DOI: 10.1016/S0040-4039(00)73985-2 SCOPUS: 2-s2.0-0027179077 WoS: WOS:A1993LT95100038 GOOGLE SCHOLAR

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Abstract

The 3-amino-2-alkenimines 1 are photochemically reactives. Their irradiation in solution (tetrahydrofuran, methanol, diethyl ether, toluene) produces substituted quinolines 2 in good to acceptable yields. A six electron electrocyclic process is proposed.