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Copper‐Catalyzed Reaction of Aryl Isocyanides with Active Methylene Isocyanides and Arylsulfonothioates: Synthesis of Sulfur‐Containing Trisubstituted Imidazoles.
- Source :
-
Advanced Synthesis & Catalysis . 11/5/2019, Vol. 361 Issue 21, p4909-4913. 5p. - Publication Year :
- 2019
-
Abstract
- A Copper‐catalyzed reaction of aryl isocyanides with active methylene isocyanides and arylsulfonothioates is developed for the synthesis of sulfur‐containing trisubstituted imidazoles. This reaction not only forms new C−C, C−N, and C−S bonds in one step, but also provides a new strategy for the construction of trisubstituted imidazoles based on the isocyanide‐isocyanide [3+2] cycloaddition. [ABSTRACT FROM AUTHOR]
- Subjects :
- *ISOCYANIDES
*RING formation (Chemistry)
*IMIDAZOLES
Subjects
Details
- Language :
- English
- ISSN :
- 16154150
- Volume :
- 361
- Issue :
- 21
- Database :
- Academic Search Index
- Journal :
- Advanced Synthesis & Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 139521458
- Full Text :
- https://doi.org/10.1002/adsc.201900904