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2.beta.-Methoxy-Clovan-9-one
SpectraBase Compound ID BXWFJBbV5Fg
InChI InChI=1S/C16H26O2/c1-14(2)9-13(18-4)16-8-6-12(17)15(3,10-16)7-5-11(14)16/h11,13H,5-10H2,1-4H3/t11-,13-,15+,16-/m0/s1
InChIKey OPOZLLBXDVIYTB-YUDUHTQSSA-N
Mol Weight 250.38 g/mol
Molecular Formula C16H26O2
Exact Mass 250.19328 g/mol
Enantiomer InChIKey OPOZLLBXDVIYTB-XABYNWHXSA-N
Copyright Copyright © 2024-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-61-1350-3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-BETA-METHOXY-9-OXOClOVANE
  • (1S,2S,5S,8R)-2-methoxy-4,4,8-trimethyltricyclo[6.3.1.0(1,5)]dodecan-9-one
Title Journal or Book Year
Structure−Activity Relationships in the Fungistatic Activity against Botrytis cinerea of Clovanes Modified on Ring C Journal of Natural Products 2004
The microbiological hydroxylation of some 2,9-dioxygenated clovanes by Mucor plumbeus Phytochemistry 1999
The Biotransformation of Some Clovanes by Botrytis cinerea Journal of Natural Products 1998

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