N-cyclopropylimine-1-pyrroline rearrangement. A novel photochemical reaction

  1. Campos, P.J. 1
  2. Soldevilla, A. 1
  3. Sampedro, D. 1
  4. Rodríguez, M.A. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Aldizkaria:
Organic Letters

ISSN: 1523-7060

Argitalpen urtea: 2001

Alea: 3

Zenbakia: 25

Orrialdeak: 4087-4089

Mota: Artikulua

DOI: 10.1021/OL016847X SCOPUS: 2-s2.0-0011453965 WoS: WOS:000172602200027 GOOGLE SCHOLAR

Beste argitalpen batzuk: Organic Letters

Gordailu instituzionala: lock_openSarbide irekia Editor

Laburpena

matrix presented A novel aza-(vinylcyclopropane-cyclopentene) photochemical rearrangement is reported. 1-Pyrrolines are easily synthesized in good yields from N-cyclopropylimines. Hydrogen, alkyl, and aryl groups can be placed anywhere within the system, and the reaction proceeds regiospecifically.