Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5273325 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
A macrocyclic bis-malonate incorporating two rigid di(phenylethynyl)silane moieties has been prepared and used to functionalize C60 in a double Bingel cyclopropanation. Two regioisomeric bis-adducts have been thus obtained, namely the trans-1 and trans-3 isomers. The formation of these specific isomers is favored by both the size of the starting macrocycle and the minimum of strain in the final products.
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