Synthetic and Computational Studies on Symmetry-Defined Double Cycloaddition of a New Tris-Annulating Reagent to C60
- 1 July 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (15), 5034-5041
- https://doi.org/10.1021/jo970685u
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Biological applications of fullerenesBioorganic & Medicinal Chemistry, 1996
- In vivo biological behavior of a water-miscible fullerene: 14C labeling, absorption, distribution, excretion and acute toxicityChemistry & Biology, 1995
- Polar Superstructures Stabilized by Polymeric Oxometal Units: Columnar Liquid Crystals Based on Tapered Dioxomolybdenum ComplexesAngewandte Chemie International Edition in English, 1994
- Regiochemistry of Multiple Additions to the Fullerene Core: Synthesis of a Th-Symmetric Hexakis adduct of C60 with Bis(ethoxycarbonyl)methyleneJournal of the American Chemical Society, 1994
- [1 + 2] and [3 + 2] cycloaddition reactions of vinylcarbenes with C60Tetrahedron Letters, 1993
- Photoinduced biochemical activity of fullerene carboxylic acidJournal of the American Chemical Society, 1993
- Chemical derivatization of organofullerenes through oxidation, reduction, and carbon-oxygen and carbon-carbon bond-forming reactionsThe Journal of Organic Chemistry, 1993
- Intramolecular alkene trapping of pyran-4-one-derived Zwitterions: a novel synthesis of diquinanes and hydrindansJournal of the American Chemical Society, 1993
- Thermal reactions of substituted cyclopropenone acetals. Regio- and stereochemistry of vinylcarbene formation and low-temperature [3 + 2] cycloadditionJournal of the American Chemical Society, 1992
- General synthesis of cyclopropenones and their acetalsTetrahedron, 1992