Mono- and Penta-Addition of Enol Silyl Ethers to [60]Fullerene
Author:
Affiliation:
1. Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol8020379
Reference38 articles.
1. Reversible Template-Directed Activation of Equatorial Double Bonds of the Fullerene Framework: Regioselective Direct Synthesis, Crystal Structure, and Aromatic Properties ofTh-C66(COOEt)12
2. C60 Hexakisadducts with an Octahedral Addition Pattern − A New Structure Motif in Organic Chemistry
3. Synthesis of [60]fullerene derivatives with an octahedral addition pattern
4. Regio- and Diastereoselective Bisfunctionalization of C60 and Enantioselective Synthesis of a C60 Derivative with a Chiral Addition Pattern
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1. Synthesis of Cs-symmetrical C60 tetra-adducts via reactions of C60Cl6 with CH-acids and enol silyl ester;Organic & Biomolecular Chemistry;2024
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