Back to Search
Start Over
N-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction via α-C(sp3)–H activation strategy.
N-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction via α-C(sp3)–H activation strategy.
- Source :
- Chemical Communications; 7/18/2024, Vol. 60 Issue 56, p7180-7183, 4p
- Publication Year :
- 2024
-
Abstract
- A novel process using N-benzylhydroxylamine hydrochloride as a "C1N1 synthon" in [2+2+1] cyclization for the construction of 1,2,5-trisubstituted imidazoles has been described for the first time. The key to realizing this process lies in capturing arylamines by in situ generated novel acyl ketonitrone intermediates. Subsequent tautomerization activates the α-C(sp<superscript>3</superscript>)–H of N-benzylhydroxylamines, and thus breaks through its inherent reaction mode and achieves N, α-C site-selective cyclization. Furthermore, this method enables scale-up synthesis and late-stage modification of complex molecules. [ABSTRACT FROM AUTHOR]
- Subjects :
- AROMATIC amines
RING formation (Chemistry)
MOLECULES
Subjects
Details
- Language :
- English
- ISSN :
- 13597345
- Volume :
- 60
- Issue :
- 56
- Database :
- Complementary Index
- Journal :
- Chemical Communications
- Publication Type :
- Academic Journal
- Accession number :
- 178338939
- Full Text :
- https://doi.org/10.1039/d4cc02105c