Towards sixfold functionalization of buckminsterfullerene (C60) at fully addressable octahedral sites

Angewandte Chemie - International Edition

Volumn 38, Issue 16, 1999, Pages 2356-2360

  Qian, Wenyuan ^a   Rubin, Yves ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cycloadditions; Diels Alder reactions diimines; Fullerenes; Semiempirical calculations

Indexed keywords

FULLERENE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHROMATOGRAPHY; CYCLIZATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; THIN LAYER CHROMATOGRAPHY;

EID: 0033549811     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19990816)38:16<2356::AID-ANIE2356>3.0.CO;2-Y     Document Type: Article

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