SYNTHESIS OF 5-HYDROXY-3-TRIFLUOROMETHYL-PYRAZOLES BY RING OPENING OF 3-TRIFLUOROACETYL-BENZOLACTAMS
β Scribed by J. P. Bouillon; Z. Janousek; H. G. Viehe; B. Tinant; J. P. Declercq
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 611 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0037-9646
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Two new series of 1,1 0 -carbonyl-bis[3-aryl(heteroaryl)-5-trihalomethyl-1H-pyrazoles], where aryl ΒΌ C 6 H 5 , 4-CH 3 C 6 H 4 , 4-FC 6 H 4 , 4-OCH 3 C 6 H 4 , 4-NO 2 C 6 H 4 , 4,4 0 -BiPh, 1-naphthyl, and heteroaryl ΒΌ 2thienyl and 2-furyl have been synthesized, in a one-pot methodology, from the rea
Intramolecular carbene lnsertlon' In tiamantane could give rise, In prlnclple, to two different dehydrodlamantanes, the 1,3 (Ia) and 3,5 (To) isomers, by analogy with slmllar behavior m the adamantane2 and homoadamantanes series. In order to establish the course of this