A highly efficient and simple one-pot procedure to synthesize 3,4-dihydro-pyrano[4,3-b]quinolin-1-ones via Rh(III)-catalysed [4 + 2] redox annulation of 3-carboxyquinolines with internal alkynes has been developed. This reaction features the generality of a broad scope of substrates, avoidance of external oxidants, high atom-economy and excellent regioselectivity.
Z. Yang, C. Pi, X. Cui and Y. Wu, Org. Chem. Front., 2019, 6, 2897 DOI: 10.1039/C9QO00710E
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...
