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#6;[4AR-(4A-ALPHA,4B-BETA,8A-ALPHA,10A-BETA)]-7-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2,4B,8,10A-TETRAMETHYL-4A,4B,5,6,8A,9,10,10A-OCTAHYDRO-1-(4H)-PHENANTHRENONE

Compound with spectra: 1 NMR, and 1 MS (GC)

#6;[4AR-(4A-ALPHA,4B-BETA,8A-ALPHA,10A-BETA)]-7-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2,4B,8,10A-TETRAMETHYL-4A,4B,5,6,8A,9,10,10A-OCTAHYDRO-1-(4H)-PHENANTHRENONE
SpectraBase Compound ID KJMXW0OkwuF
InChI InChI=1S/C24H40O2Si/c1-16-10-11-20-23(6)15-13-19(26-27(8,9)22(3,4)5)17(2)18(23)12-14-24(20,7)21(16)25/h10,18,20H,11-15H2,1-9H3/t18-,20+,23-,24+/m0/s1
InChIKey ABEVIAWTQRWUNE-GONLTWLXSA-N
Mol Weight 388.7 g/mol
Molecular Formula C24H40O2Si
Exact Mass 388.279757 g/mol
Enantiomer InChIKey ABEVIAWTQRWUNE-ZOGBDMNLSA-N

View Spectrum of #6;[4AR-(4A-ALPHA,4B-BETA,8A-ALPHA,10A-BETA)]-7-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2,4B,8,10A-TETRAMETHYL-4A,4B,5,6,8A,9,10,10A-OCTAHYDRO-1-(4H)-PHENANTHRENONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-63-5105-6

View Spectrum of #6;[4AR-(4A-ALPHA,4B-BETA,8A-ALPHA,10A-BETA)]-7-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-2,4B,8,10A-TETRAMETHYL-4A,4B,5,6,8A,9,10,10A-OCTAHYDRO-1-(4H)-PHENANTHRENONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • [4aR-(4a.alpha.,4b.beta.,8a.alpha.,10a.beta.-)]-7-[(tert-Butyldimethylsilyl)oxy]-2,4b,8,10a-tetramethyl-4a.4b,5,6,8a,9,10,10a-octahydro-1(4H)-phenanthrenone
METHYL-(1R-(1-ALPHA,4A-BETA,4B-ALPHA,7-ALPHA,10A-ALPHA))-1,2,3,4,4A,4B,5,6,7,8,10,10A-DODECAHYDRO-7-HYDROXY-1,4A-DIMETHYL-7-(1-METHYLETHY
4-ALPHA-HYDROXYDEMETHYLPLAKINAMINE-B
Ent-cis-clerodane dilactone
AMPHIACROLIDE-F
No Name
25-Acetoxy-cholest-4-ene-3,6-dione
4-ALPHA-CARBOXY-1-ALPHA,13-ALPHA-DIHYDROXY-13,16-SECO-ENT-19-NORBEYERAN-16-OIC_ACID_13,16-LACTONE
7.BETA.-[(TRIMETHYLSILYL)OXY]-5.ALPHA.-ANDROSTAN-3,17-DIONE(3,17-DI-O-METHYLOXIME)
[3S-(3-ALPHA,3A-ALPHA,5AS,7A-ALPHA,11A-BETA,11B-ALPHA)]-1,3,3A,6,7,7A,8,9,10,11,11A,11B-DODECAHYDRO-3,3-(EPOXYMETHANO)-8,8,11A-TRIMETHYLCYCLOBUTA-[J]-PHENANTHR
ENT-13,16-BETA-DIHYDROXY-KAURAN-19-OIC-ACID
Title Journal or Book Year
An Efficient Stereoselective Synthesis of Stypodiol and Epistypodiol The Journal of Organic Chemistry 1998
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