Abstract
The reaction of ketohydrazones containing an α-methylene group with chloramine-T followed by treatment with triethylamine leads to the formation of azoalkenes via an α-chloroazo-compound, which can react intermolecularly and in situ with olefinic compounds to produce tetrahydropyridazine derivatives in good yield.
Original language | English |
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Pages (from-to) | 5969-5970 |
Number of pages | 2 |
Journal | Tetrahedron Letters |
Volume | 46 |
Issue number | 35 |
DOIs | |
Publication status | Published - 29-08-2005 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Organic Chemistry
- Drug Discovery