Cyclopropanierung von Fullerenen
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[1] F. Diederich,et al. Improved purification of C60 and formation of σ- and π-homoaromatic methano-bridged fullerenes by reaction with alkyl diazoacetates , 1993 .
[2] K. Müllen,et al. Reaction of Buckminsterfullerene with ortho‐Quinodimethane: a New Access to Stable C60 Derivatives , 1993 .
[3] Y. Rubin,et al. Synthesis and X-ray structure of a Diels-Alder adduct of C60 , 1993 .
[4] Klaus Müllen,et al. Umsetzung von Buckminsterfulleren C60 mit ortho-Chinodimethan: ein neuer Zugang zu stabilen C60-Derivaten† , 1993 .
[5] A. Hirsch,et al. Product Predictions for Nucleophilic Additions toC70 , 1992 .
[6] A. Hirsch,et al. Produktvoraussagen bei nucleophilen Additionen an C70 , 1992 .
[7] A. Balch,et al. Structure of a Product of Double Addition to C70: [C70{Ir(CO)Cl(PPhMe2)2}2]·3C6H6 , 1992 .
[8] F. Diederich,et al. Fullerene Sugars: Preparation of Enantiomerically Pure, Spiro‐Linked C‐Glycosides of C60 , 1992 .
[9] A. Balch,et al. Doppelte Addition eines Iridiumkomplexes an C70: [C70{Ir(CO)CI(PPhMe2)2}2] · 3C6H6 , 1992 .
[10] Andrea Vasella,et al. Fullerenzucker: Herstellung enantiomerenreiner, spiroverknüpfter C-Glycoside von C60† , 1992 .
[11] F. Wudl,et al. Dihydrofulleroid HC: Synthesis and properties of the parent fulleroid , 1992 .
[12] Heinrich R. Karfunkel,et al. Titration von C60: eine Methode zur Synthese von Organofullerenen , 1992 .
[13] A. Hirsch,et al. Titration of C60: A Method for the Synthesis of Organofullerenes , 1992 .
[14] Tibor Braun. Die epidemische Ausbreitung der Fulleren-Forschung† , 1992 .
[15] Tibor Braun,et al. The Epidemic Spread of Fullerene Research , 1992 .
[16] F. Wudl. The chemical properties of buckminsterfullerene (C60) and the birth and infancy of fulleroids , 1992 .
[17] W. Krätschmer,et al. Solid C60: a new form of carbon , 1990, Nature.
[18] E. Vogel,et al. Ein Aromat‐Olefin‐Gleichgewicht: 1,6‐Methano‐[10]annulen‐Tricyclo[4.4.1.0.1,6]‐undeca‐2,4,7,9‐tetraen‐Valenztautomerie , 1973 .
[19] W. Bremser,et al. An Aromatic-Olefin Equilibrium: 1,6-Methano[10]annulene-Tricyclo[4.4.l.01,6]undeca-2,4,7,9-Tetraene Valence Tautomerism† , 1973 .
[20] L. L. Mccoy. Three-membered Rings. The Preparation of Some 1,2-Cyclopropanedicarboxylic Acids , 1958 .