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Iron(II) bromide-catalyzed intramolecular C-H bond amination [1,2]-shift tandem reactions of aryl azides.

ABSTRACT: Iron(II) bromide catalyzes the transformation of ortho-substituted aryl azides into 2,3-disubstituted indoles through a tandem ethereal C-H bond amination [1,2]-shift reaction. The preference for the 1,2-shift component of the tandem reaction was established to be Me < 1° < 2° < Ph.

SUBMITTER: Nguyen Q

PROVIDER: S-EPMC3622273 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

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Iron(II) bromide-catalyzed intramolecular C-H bond amination [1,2]-shift tandem reactions of aryl azides.

Nguyen Quyen Q Nguyen Tuyen T Driver Tom G TG

Journal of the American Chemical Society 20130103 2

Iron(II) bromide catalyzes the transformation of ortho-substituted aryl azides into 2,3-disubstituted indoles through a tandem ethereal C-H bond amination [1,2]-shift reaction. The preference for the 1,2-shift component of the tandem reaction was established to be Me < 1° < 2° < Ph. ...[more]

PMID: 23265139

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