Regioselective Synthesis of Dialky1-1,3-cyclopentadienes via Novel 2-Alkyl-6,6-dialkylfulvenes
- UNCG Author/Contributor (non-UNCG co-authors, if there are any, appear on document)
- Terence "Terry" Nile, Professor (Creator)
- Institution
- The University of North Carolina at Greensboro (UNCG )
- Web Site: http://library.uncg.edu/
Abstract: 2-Alkyl-6,6-dialkylfulvenes are synthesized by the condensation of monosubstituted 1,3-cyclopentadienes with carbonyl compounds in the presence of pyrrolidine and converted to the corresponding dialkyl-1,3-cyclopentadienes by the addition of nucleophilic reagents lithium aluminum hydride or methyllithium.
Regioselective Synthesis of Dialky1-1,3-cyclopentadienes via Novel 2-Alkyl-6,6-dialkylfulvenes
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Created on 4/20/2011
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Additional Information
- Publication
- Synlett, 10, 589 (1990).
- Language: English
- Date: 1990
- Keywords
- Carbonyl compounds, pyrrolidine, methyllithium, synthesis