Regioselective synthesis of pyrazoles via the ring cleavage of 3-substituted N-alkylated 3-hydroxyisoindolin-1-ones
Cited 0 time in 
Metadata Downloads
- Title
- Regioselective synthesis of pyrazoles via the ring cleavage of 3-substituted N-alkylated 3-hydroxyisoindolin-1-ones
- Author(s)
- Kyu Tae Chang; Yong Hyun Choi; Seung Ho Kim; Yong Jin Yoon; Woo Song Lee
- Bibliographic Citation
- Journal of Chemical Society, Perkin Transaction 1, vol. 2002, no. 2, pp. 207-210
- Publication Year
- 2002
- Abstract
- The regioselective synthesis of pyrazoles via the ring cleavage of 3-substituted N-alkylated 3-hydroxyisoindolin-1-ones was reported. A one-pot addition-decyclisation-cyclocondensation process was employed in the analysis. The N-tert-butyl group was found to be the best for producing the α-acetylenic ketone intermediate.
- Keyword
- condensationketonessubstitution reactionssynthesis (chemical)regioselective synthesisaromatic hydrocarbons
- ISSN
- 1472-7781
- Publisher
- Royal Soc Chem
- Full Text Link
- http://dx.doi.org/10.1039/b108485m
- Type
- Article
- Appears in Collections:
- Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
- Files in This Item:
There are no files associated with this item.
Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.