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Catalytic enantioselective 1,3-dipolar cycloadditions of nitrones with propioloylpyrazoles and acryloylpyrazoles induced by chiral [pi]-cation catalysts
- Source :
- Journal of the American Chemical Society. Nov 10, 2010, Vol. 132 Issue 44, 15550-15552
- Publication Year :
- 2010
-
Abstract
- The enantioselective catalysis of 1,3-dipolar cycloaddition reaction of nitrones with propioloylpyrazole and acryloylpyrazole derivatives in presence of a chiral copper(II) complex of 3-(2-naphthyl)-L-alanine amide is described. The reaction is the first successful method for the catalytic enantioselective 1,3-dipolar cycloaddition of nitrones with acetylene derivatives.
- Subjects :
- Acetylene -- Chemical properties
Copper -- Chemical properties
Ring formation (Chemistry) -- Analysis
Naphthalene -- Structure
Naphthalene -- Chemical properties
Organometallic compounds -- Structure
Organometallic compounds -- Chemical properties
Pyrazoles -- Structure
Pyrazoles -- Chemical properties
Chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 00027863
- Volume :
- 132
- Issue :
- 44
- Database :
- Gale General OneFile
- Journal :
- Journal of the American Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.244916263