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(5-ALPHA,13-ALPHA,14-BETA)-14,17-EPOXY-23-HYDROXY-4,4,8-TRIMETHYL-16,24-CYCLO-13,17-SECOCHOLA-16,20(22),23-TRIEN-3-ONE

Compound with spectra: 1 NMR

(5-ALPHA,13-ALPHA,14-BETA)-14,17-EPOXY-23-HYDROXY-4,4,8-TRIMETHYL-16,24-CYCLO-13,17-SECOCHOLA-16,20(22),23-TRIEN-3-ONE
SpectraBase Compound ID BD2p3CxhBEv
InChI InChI=1S/C27H38O3/c1-16-13-19(28)14-18-15-27(30-23(16)18)17(2)7-8-21-25(5)11-10-22(29)24(3,4)20(25)9-12-26(21,27)6/h13-14,17,20-21,28H,7-12,15H2,1-6H3/t17-,20-,21+,25-,26+,27+/m0/s1
InChIKey OQOGUNVGUJIIKN-WPMRXPNTSA-N
Mol Weight 410.6 g/mol
Molecular Formula C27H38O3
Exact Mass 410.282095 g/mol
Enantiomer InChIKey OQOGUNVGUJIIKN-SUMYGZTCSA-N

View Spectrum of (5-ALPHA,13-ALPHA,14-BETA)-14,17-EPOXY-23-HYDROXY-4,4,8-TRIMETHYL-16,24-CYCLO-13,17-SECOCHOLA-16,20(22),23-TRIEN-3-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(5.alpha.,13.alpha.)-14,17-Epoxy-23-hydroxy-4,4,8-trimethyl-16,24-cyclo-13,17-secochola-16,20(22)-23-trien-3-one
Title Journal or Book Year
An Efficient Stereoselective Synthesis of Stypodiol and Epistypodiol The Journal of Organic Chemistry 1998

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