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3-ALPHA-HYDROXY-17A-OXA-D-HOMO-5-ALPHA-ANDROSTAN-17-ONE
SpectraBase Compound ID 1MnjM6SppEO
InChI InChI=1S/C19H30O3/c1-18-9-7-13(20)11-12(18)3-4-14-15(18)8-10-19(2)16(14)5-6-17(21)22-19/h12-16,20H,3-11H2,1-2H3/t12-,13+,14+,15-,16-,18-,19-/m0/s1
InChIKey SZKJPNYYJWKGMH-IUHHSCQESA-N
Mol Weight 306.45 g/mol
Molecular Formula C19H30O3
Exact Mass 306.219495 g/mol
Enantiomer InChIKey SZKJPNYYJWKGMH-YZLVVKDKSA-N
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 CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Title Journal or Book Year
Baeyer-Villiger Oxidation of Some C19 Steroids by Penicillium lanosocoeruleum Molecules 2013
Transformation of some 3α-substituted steroids by Aspergillus tamarii KITA reveals stereochemical restriction of steroid binding orientation in the minor hydroxylation pathway The Journal of Steroid Biochemistry and Molecular Biology 2010
Transformation of a series of saturated isomeric steroidal diols by Aspergillus tamarii KITA reveals a precise stereochemical requirement for entrance into the lactonization pathway The Journal of Steroid Biochemistry and Molecular Biology 2010

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