(Figure Presented) Thermodynamically driven epimerization at the trindane benzylic positions of "hexacarboxytrindanes" generates benzene rings with D3 symmetry and with R or S homotopic faces. Almost total resolution towards S trindanes was achieved by epimerization and transesterification with lithium (-)-mentholate. These structures are attractive cores for the construction of macromolecules in which asymmetry is induced by the center of the molecule. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
Autori: | |
Data di pubblicazione: | 2005 |
Titolo: | "Hexacarboxytrindanes": Benzene rings with homotopic faces as scaffolds for the construction of D-3 chiral architectures |
Rivista: | ANGEWANDTE CHEMIE. INTERNATIONAL EDITION |
Digital Object Identifier (DOI): | http://dx.doi.org/10.1002/anie.200502262 |
Volume: | 44 |
Appare nelle tipologie: | 2.1 Articolo su rivista |
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