ISSN:
1434-193X
Keywords:
Chirality
;
Dendrimers
;
Fullerenes
;
Lipofullerenes
;
Chemistry
;
General Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
---The facile synthesis of enantiomerically pure C3-symmetrical fullerene dendrimers all-R-fA-7, all-S-fC-8, all-R-fC-9, and all-S-fA-10, as well as lipofullerenes all-S-fA-11 and all-S-fC-12 involving an octahedral [3:3] addition pattern is described. The C3 symmetrical tris[bis(4-phenyl-2-oxazoline)methano]fullerenes 1, 2, 3, and 4 with known absolute configuration were used as precursors. The completion of the octahedral addition pattern was achieved by a threefold cyclopropanation with the dendritic 3,5-dihydroxybenzylic bromomalonate 5 and the lipophilic dioctadecyl bromomalonate 6. The absolute configurations of the precursor trisadducts were retained in the inherently chiral C3-symmetrical hexakisadducts 7-12. The structure and the isomeric purity of all hexakisadducts 7-12 were unambiguously proven by NMR spectroscopy and other techniques. Preliminary experiments with the dendritic hexakisadducts all-S-fC 8 and all-S-fA 10 revealed that these macromolecular ligands posess catalytic properties with respect to stereoselective cyclopropanations of styrene with ethyl diazoacetate.
Additional Material:
6 Ill.
Type of Medium:
Electronic Resource
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