Synthesis of Fluoroazaindolines by an Uncommon Radical ipso Substitution of a Carbon−Fluorine Bond
Author:
Affiliation:
1. Laboratoire de Synthèse Organique, UMR 7652 CNRS/Ecole Polytechnique, 91128 Palaiseau, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol101240f
Reference43 articles.
1. Tin-Free Radical Cyclizations for the Synthesis of 7-Azaoxindoles, 7-Azaindolines, Tetrahydro[1,8]naphthyridines, and Tetrahydro-5H-pyrido[2,3-b]azepin-8-ones
2. An unprecedented radical ring closure on a pyridine nitrogen
3. We wish to acknowledge in this respect our collaboration on the theoretical aspects with Dr. Michelle Coote at the Australian National University.
4. For reviews on xanthate chemistry, see:
5. The Degenerative Radical Transfer of Xanthates and Related Derivatives: An Unusually Powerful Tool for the Creation of Carbon–Carbon Bonds
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