Selective Functionalization on [60]Fullerene Governed by Tether Length
- 1 February 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (5) , 926-932
- https://doi.org/10.1021/ja960873m
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Regio- and diastereo-controlled double cycloaddition to [60] fullerene: one-step synthesis of Cs and C2 chiral organofullerenes with new tris-annulating reagentsChemical Communications, 1996
- Relaxation processes in the excited state of C60–o-quinodimethane adductsJournal of the Chemical Society, Faraday Transactions, 1996
- Synthesis and electronic properties of C60–o-quinodimethane adductsJournal of the Chemical Society, Perkin Transactions 2, 1995
- Tether‐Directed Remote Functionalization of Buckminsterfullerene: Regiospecific Hexaadduct FormationAngewandte Chemie International Edition in English, 1994
- C60H4: Kinetics and Thermodynamics of Multiple Addition to C60Angewandte Chemie International Edition in English, 1994
- Synthesis and properties of a novel redox system containing fullerene and p-benzoquinoneJournal of the Chemical Society, Chemical Communications, 1994
- A Diels–Alder adduct of C60containing hydroxyquinone functionalitiesJournal of the Chemical Society, Chemical Communications, 1994
- Reaction of Buckminsterfullerene with ortho‐Quinodimethane: a New Access to Stable C60 DerivativesAngewandte Chemie International Edition in English, 1993
- Isolation and characterization of Diels–Alder adducts of C60with anthracene and cyclopentadieneJournal of the Chemical Society, Chemical Communications, 1993
- C60‐Fullerene—A Playground for Chemical Manipulations on Curved Surfaces and in Cavities**Angewandte Chemie International Edition in English, 1992