Diastereoselective Construction of 2-Aminoindanones via an In(OTf)3-Catalyzed Domino Reaction.
J Org Chem
; 84(14): 8984-8997, 2019 Jul 19.
Article
em En
| MEDLINE
| ID: mdl-31250644
ABSTRACT
An In(OTf)3-catalyzed domino reaction involving sequential oxidative ring opening of aziridines by using the solvent dimethyl sulfoxide and intramolecular Michael addition has been developed for the modular synthesis of 2-aminoindanone compounds by the formation of one new CâO bond and one new C-C bond. The notable feature of this strategy includes broad substrate scope, excellent trans-diastereoselectivities, highly functionalized products, and mild conditions. The catalyst In(OTf)3 plays an important role in the formation of the indanone ring.
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1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
J Org Chem
Ano de publicação:
2019
Tipo de documento:
Article