Unknown

Dataset Information

0

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

altmetric image

Publications

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]

Similar Datasets

| S-EPMC2743533 | biostudies-literature
| S-EPMC2913475 | biostudies-literature
| S-EPMC5802275 | biostudies-other
| S-EPMC6429596 | biostudies-literature
| S-EPMC8159214 | biostudies-literature
| S-EPMC7898293 | biostudies-literature
| S-EPMC3148652 | biostudies-literature