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BIADAMANTYLIDENE
SpectraBase Compound ID BXhhrOZPQLw
InChI InChI=1S/C20H28/c1-11-3-15-5-12(1)6-16(4-11)19(15)20-17-7-13-2-14(9-17)10-18(20)8-13/h11-18H,1-10H2/b20-19-/t11-,12+,13-,14+,15-,16+,17-,18+
InChIKey KRDXURLKZNAXAQ-WKXKSFOSSA-N
Mol Weight 268.44 g/mol
Molecular Formula C20H28
Exact Mass 268.219101 g/mol
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent BE
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD2Cl2
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
  • KRDXURLKZNAXAQ-WKXKSFOSSA-N
  • Adamantylidene-adamantane
  • TRICYCLO[3.3.1.1(3,7)]DECANE, TRICYCLO[3.3.1.1(3,7)]DECYLIDENE-
  • [2,2']Biadamantanylidene
Title Journal or Book Year
Protonation studies on epimeric homoallylic adamantylideneadamantyl alcohols, 4-methyleneadamantylideneadamantane, adamantylideneadamantane (AdAd) and sesquihomoadamantene, and reaction of AdAd and sesquihomoadamantene with NO2+BF4– and PhI(OH)OTs: a stable-ion NMR and theoretical (GIAO-NMR) studyElectronic supplementary information (ESI) available: representative 1D-NMR spectra and tables of cartesian coordinates. See http://www.rsc.org/suppdata/p2/b2/b201660e/ Journal of the Chemical Society, Perkin Transactions 2 2002
σ,π Interaction in Halogen-Substituted Biadamantylidene Radical Cations The Journal of Organic Chemistry 1997
Stable Bromonium and Iodonium Ions of the Hindered Olefins Adamantylideneadamantane and Bicyclo[3.3.1]nonylidenebicyclo[3.3.1]nonane. X-Ray Structure, Transfer of Positive Halogens to Acceptor Olefins, and ab Initio Studies Journal of the American Chemical Society 1994

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