A novel synthesis of 3,4-disubstituted cinnolines from o-trifluorophenyl hydrazones
โ Scribed by Alexander S. Kiselyov; Celia Dominguez
- Book ID
- 104261732
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 235 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
An efficient synthesis of 3-aryl-4-aminocinnolines from ortho-trifluoromethylphenyl hydrazones is described.
The mechanism of the described transformation is likely to involve the formation of the quinone methide intermediate. The described procedure is easily adaptable to automated solid phase synthesis leading to analytically pure heterocycles.
๐ SIMILAR VOLUMES
A new method for the stereospecific synthesis of cis-3,4-disubstituted cyclopentanones is described. 4s a part of synthetic studies on biologically active compounds consisting of five membered ring such as prostaglandins, brefeldin A and methylenomycin A, we undertook the stereospecific synthesis of