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Gold-catalyzed (4+3)-annulations of 2-alkenyl-1-alkynylbenzenes with anthranils with alkyne-dependent chemoselectivity: skeletal rearrangement versus non-rearrangement

Two distinct (4+3)-nitroxy annulations between 1,5-enynes and anthranils have been developed to access tetrahydro-1H-benzo[b]azepine derivatives; the chemoselectivity varies with the types of alkynes. Terminal alkyne substrates deliver benzo[b]azepine derivatives via a novel skeletal rearrangement w...

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Detalles Bibliográficos
Autores principales: Singh, RahulKumar Rajmani, Skaria, Manisha, Chen, Liang-Yu, Cheng, Mu-Jeng, Liu, Rai-Shung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349068/
https://www.ncbi.nlm.nih.gov/pubmed/30774919
http://dx.doi.org/10.1039/c8sc03619e