Ring-Rearrangement Metathesis of 1-Substituted 7-Azanorbornenes as an Entry to 1-Azaspiro[4.5]decane systems

  1. Carreras, J. 1
  2. Avenoza, A. 1
  3. Busto, J.H. 1
  4. Peregrina, J.M. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Aldizkaria:
Journal of Organic Chemistry

ISSN: 0022-3263

Argitalpen urtea: 2011

Alea: 76

Zenbakia: 9

Orrialdeak: 3381-3391

Mota: Artikulua

DOI: 10.1021/JO200321T SCOPUS: 2-s2.0-79955554628 WoS: WOS:000289956900044 GOOGLE SCHOLAR

Beste argitalpen batzuk: Journal of Organic Chemistry

Lotura duten proiektuak

Síntesis y análisis conformacional de O-Glicopéptidos de interés estructural y biológico.

2009/00205/001

Laburpena

Several metathesis sequences have been carried out using 7-azanorbornenes as starting materials. The occurrence of several exocyclic olefin patterns in the bridgehead position of this system opens the way to gain interesting spirocyclic compounds, which were achieved using several ring-rearrangement metatheses (RRM). The metathesis products, thus obtained, may be useful for the synthesis of new peptidomimetics and related compounds. © 2011 American Chemical Society.