Diastereoselective Pentadienylation Reaction of Protected Chiral alpha-Amino Aldehydes
Diastereoselective pentadienylation of chiral α-amino aldehydes was achieved. The obtained anti amino alcohols can be transformed into dienic imines which undergo Diels-Alder cyclisation to give stereoselectively indolizidines.
Références
- Titre
- Diastereoselective Pentadienylation Reaction of Protected Chiral alpha-Amino Aldehydes
- Type de publication
- Article de revue
- Année de publication
- 2000
- Auteurs
- Minassian, Frédéric, Pelloux-Leon Nadia, and Vallee Yannick.
- Revue
- Synlett
- Volume
- 2000
- Pagination
- 242–244
- ISSN
- 0936-5214
Soumis le 11 juillet 2019