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• W2076842281 abstract "Abstract The Bingel addition of a trimalonate derived from a chiral, cyclotriveratrylene (CTV)‐based tripodal tether to C 60 was reinvestigated. The present use of enantiomerically pure ( P )‐ and ( M )‐configured CTV units in the tether allowed the isolation of a total of four enantiomerically pure C 3 ‐symmetric tris‐adducts of [60]fullerene (two from each CTV enantiomer). With the support of NMR and UV/Vis spectroscopy, electronic (ECD) and vibrational (VCD) circular dichroism spectroscopic analysis (comparison to ECD data of known compounds and to ECD and VCD data calculated by TD‐DFT or ZINDO methods as part of this work) allowed a definitive determination of the following structural features for all four CTV‐C 60 conjugates: (i) The constitution of the fullerene addition pattern, (ii) its absolute configuration, and (iii) the absolute configuration of the CTV moiety. It is concluded that the triple Bingel addition proceeded with complete regioselectivity and negligible diastereoselectivity, affording only the trans ‐3, trans ‐3, trans ‐3 fullerene addition pattern in both enantiomeric forms, whereas the previously reported e , e , e motif was not formed." @default.
• W2076842281 created "2016-06-24" @default.
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• W2076842281 date "2010-08-01" @default.
• W2076842281 modified "2023-10-09" @default.
• W2076842281 title "Regioselectivity in Tether‐Directed Remote Functionalization – The Addition of a Cyclotriveratrylene‐Based Trimalonate to C₆₀ Revisited" @default.
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• W2076842281 doi "https://doi.org/10.1002/ejoc.201000396" @default.
• W2076842281 hasPublicationYear "2010" @default.
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