Cross-coupling of 1-aryl-5-bromopyrazoles: regioselective synthesis of 3,5-disubstituted 1-arylpyrazoles
β Scribed by Xiao-jun Wang; Jonathan Tan; Karl Grozinger
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 160 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The cross-coupling of 1-aryl-5-bromopyrazoles 4 with alkynes, vinyltins and arylboronic acids promoted by Pd(PPh 3 ) 4 aorded unsymmetrical 3,5-disubstituted 1-arylpyrazoles 5-8 in excellent yields. 1-Aryl-5bromopyrazoles 4 were prepared from their corresponding 1-arylpyrazolones 3 with PBr 3 in reΒ―uxing acetonitrile.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract Crossβcoupling of the bromides or iodides of the substituted isomeric diphenyl(methylthio)pyrazoles with a wide range or aromatic and heteroaromatic boronic acids tolerates many functional groups and affords the products with high yields.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.