Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer–Schuster Rearrangement, Anti-Michael Addition/C((sp(3)))–H Functionalization, and Azacyclization

[Image: see text] A one-pot, sequential Meyer–Schuster (MS) rearrangement of oxindole-derived propargyl alcohols to the corresponding α,β-unsaturated enones and their anti-Michael addition, followed by intramolecular azacyclization is described in a highly regioselective manner using Ca(OTf)(2) as t...

Descripción completa

Detalles Bibliográficos
Autores principales: Yaragorla, Srinivasarao, Dada, Ravikrishna, Rajesh, P., Sharma, Manju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044873/
https://www.ncbi.nlm.nih.gov/pubmed/30023853
http://dx.doi.org/10.1021/acsomega.8b00147

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044873/
https://www.ncbi.nlm.nih.gov/pubmed/30023853
http://dx.doi.org/10.1021/acsomega.8b00147

Ejemplares similares