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Regioselective Arylative Ring-Closing Reaction of 2-Alkynylphenyl Derivatives: Formation of Arylated Benzoxazin-2-ones, Benzoxazin-2-amines and 2,3-Disubstituted Indoles.
- Source :
- European Journal of Organic Chemistry; Dec2016, Vol. 2016 Issue 36, p5990-6000, 11p
- Publication Year :
- 2016
-
Abstract
- Copper-catalysed arylative ring-closing reactions of 2-alkynylphenylcarbamates and 2-alkynylphenylureas with diaryliodonium salts gave C, N-double-arylated benzoxazin-2-ones and C-arylated benzoxazin-2-amines, respectively, both bearing fully substituted exocyclic olefins. On the other hand, the palladium-catalysed arylative ring-closing reaction of 2-alkynylphenylcarbamates gave C-arylated 2,3-disubstituted indoles. [ABSTRACT FROM AUTHOR]
- Subjects :
- PHENYL compounds
BENZOXAZINES
INDOLE compounds
CHEMICAL reactions
OXAZINES
Subjects
Details
- Language :
- English
- ISSN :
- 1434193X
- Volume :
- 2016
- Issue :
- 36
- Database :
- Complementary Index
- Journal :
- European Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 120385535
- Full Text :
- https://doi.org/10.1002/ejoc.201601162