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CBr 4 ‐Mediated Cross‐Dehydrogenative Coupling Reaction of Amines
A novel CBr 4 ‐mediated dehydrogenative Povarov/aromatization tandem reaction of glycine derivatives with alkenes, leading to complex quinoline derivatives, and a CBr 4 ‐mediated dehydrogenative CH functionalization of N ‐aryl tetrahydroisoquinolines with nucleophiles to form CC and CP bonds are...
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Published in: | Chemistry : a European journal 2015-04, Vol.21 (15), p.5723-5726 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A novel CBr
4
‐mediated dehydrogenative Povarov/aromatization tandem reaction of glycine derivatives with alkenes, leading to complex quinoline derivatives, and a CBr
4
‐mediated dehydrogenative CH functionalization of
N
‐aryl tetrahydroisoquinolines with nucleophiles to form CC and CP bonds are reported. The reactions were performed under very simple and mild reaction conditions; only CBr
4
was used as a promoter. A plausible mechanism involving a radical process is proposed. |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201500453 |