Intramolecular [3 + 2]-Cycloadditions of Azomethine Ylides Derived from Secondary Amines via Redox-Neutral C–H Functionalization

[Image: see text] Azomethine ylides are accessed under mild conditions via benzoic acid catalyzed condensations of 1,2,3,4-tetrahydroisoquinolines or tryptolines with aldehydes bearing a pendent dipolarophile. These intermediates undergo intramolecular [3 + 2]-cycloadditions in a highly diastereosel...

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Detalles Bibliográficos
Autores principales: Mantelingu, Kempegowda, Lin, Yingfu, Seidel, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4251528/
https://www.ncbi.nlm.nih.gov/pubmed/25413125
http://dx.doi.org/10.1021/ol502918g

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4251528/
https://www.ncbi.nlm.nih.gov/pubmed/25413125
http://dx.doi.org/10.1021/ol502918g

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