Eine topochemisch kontrollierte, regiospezifische Fulleren‐Bisfunktionalisierung
- 3 June 1996
- journal article
- Published by Wiley in Angewandte Chemie
- Vol. 108 (11), 1294-1296
- https://doi.org/10.1002/ange.19961081108
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Ein hochsymmetrisches Produkt einer sechsfachen [4 + 2]‐Cycloaddition des C60‐FullerensAngewandte Chemie, 1995
- Spacer‐kontrollierte Fernfunktionalisierung von Buckminsterfulleren: regiospezifische Bildung eines HexaadduktesAngewandte Chemie, 1994
- Spectral Characterization of Anthracene-, Cyclopentadiene-, and Dichlorocarbene-C60AdductsFullerene Science and Technology, 1994
- Structure of C60: partial orientational order in the room-temperature modification of C60Acta crystallographica Section B, Structural science, crystal engineering and materials, 1993
- Structural chemistry in Helvetica Chimica Acta, 1917–1992Helvetica Chimica Acta, 1993
- Isolation and characterization of Diels–Alder adducts of C60with anthracene and cyclopentadieneJournal of the Chemical Society, Chemical Communications, 1993
- Synthesis, purification, and characterization of the 1 : 1 addition product of C60 and anthraceneJournal of the Chemical Society, Chemical Communications, 1993
- Strategien zum Aufbau molekularer und polymerer KohlenstoffallotropeAngewandte Chemie, 1992
- 3:1 Molecular Complex of Hydroquinone and C60Helvetica Chimica Acta, 1991
- Solid C60: a new form of carbonNature, 1990