A highly efficient and mild defluorinative methodology has been developed to synthesize various fluorinated 1,2-naphthoquinones from readily accessible o-trifluoromethylbenzylamine derivatives and enolizable esters. The resultant fluorinated 1,2-naphthoquinones are subsequently transformed into tetra-substituted indane and phenazine derivatives.
R. R. Kusmude, M. Yadav, S. A. Kale and S. Dhiman, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC01497F
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...
