Unprecedented ring expansion of [60]fullerene: incorporation of nitrogen at an open 6,6-ring juncture by regiospecific reduction of oxycarbonylaziridino-[2′,3′:1,2][60]fullerenes. Synthesis of 1a-aza-1(6a)-homo[60]fullerene, C 60 H 2 NH

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 1996 (4), p.507-508
Hauptverfasser: Banks, Malcolm R., Cadogan, J. I. G., Gosney, Ian, Henderson, Alan J., Hodgson, Philip K. G., Kerr, Wesley G., Kerth, Andreas, Langridge-Smith, Patrick R. R., Millar, John R. A., Mount, Andrew R., Parkinson, John A., Taylor, Alan T., Thornburn, Paul
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container_end_page 508
container_issue 4
container_start_page 507
container_title Chemical communications (Cambridge, England)
container_volume
creator Banks, Malcolm R.
Cadogan, J. I. G.
Gosney, Ian
Henderson, Alan J.
Hodgson, Philip K. G.
Kerr, Wesley G.
Kerth, Andreas
Langridge-Smith, Patrick R. R.
Millar, John R. A.
Mount, Andrew R.
Parkinson, John A.
Taylor, Alan T.
Thornburn, Paul
description
doi_str_mv 10.1039/CC9960000507
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source Royal Society Of Chemistry Journals; Royal Society of Chemistry Journals Archive (1841-2007); Alma/SFX Local Collection
title Unprecedented ring expansion of [60]fullerene: incorporation of nitrogen at an open 6,6-ring juncture by regiospecific reduction of oxycarbonylaziridino-[2′,3′:1,2][60]fullerenes. Synthesis of 1a-aza-1(6a)-homo[60]fullerene, C 60 H 2 NH
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