Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
171412 | Comptes Rendus Chimie | 2009 | 10 Pages |
Abstract
Two series of isomeric dyads with differently branched phenyleneethynylene-based moieties and a pyrrolidinofullerene core have been prepared. The synthetic approach to prepare these compounds relies upon the 1,3-dipolar cycloaddition of an azomethine ylide generated in situ from the corresponding aldehydes and N-methylglycine.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Michel Holler, Maxence Urbani, Aline Gégout, Sheng Zhang, Jean-François Nierengarten,