Synthesis of Enantiopure T-Symmetrical [6:0]-Hexakis Adducts of C60 Equipped with 1,2-Glycol Substituted cyclo-Monomalonate Addends
Author:
Affiliation:
1. Department of Chemistry, University of Cyprus, University Str 1, Building no. 13, 2109 Aglantzia, Nicosia, Cyprus
Funder
Cyprus Research Promotion Foundation
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b00220
Reference36 articles.
1. C60 Hexakisadducts with an Octahedral Addition Pattern − A New Structure Motif in Organic Chemistry
2. A multiply-substituted buckminsterfullerene (C60) with an octahedral array of platinum atoms
3. Regiochemistry of Multiple Additions to the Fullerene Core: Synthesis of a Th-Symmetric Hexakis adduct of C60 with Bis(ethoxycarbonyl)methylene
4. A Highly Symmetric Sixfold Cycloaddition Product of Fullerene C60
5. Reversible Template-Directed Activation of Equatorial Double Bonds of the Fullerene Framework: Regioselective Direct Synthesis, Crystal Structure, and Aromatic Properties ofTh-C66(COOEt)12
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1. A covalent organic cage compound acting as a supramolecular shadow mask for the regioselective functionalization of C60;Chemical Science;2020
2. Cycloaddition Reactions of Azomethine Ylides and 1,3-Dienes on the C2v-Symmetrical Pentakisadduct of C60;The Journal of Organic Chemistry;2018-01-30
3. Metal-Based Diversity for Crystalline Metal-Fullerene Frameworks;Chemistry - A European Journal;2017-10-10
4. Metal–organic hybrid architectures built from functionalized fullerenes and metal ions or clusters;Tetrahedron Letters;2016-10
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