2465-05-6Relevant academic research and scientific papers
1H and 13C NMR Assignments for Lanostan-3β-ol Derivatives: Revised Assignments for Lanosterol
Emmons, Gary T.,Wilson, William K.,Schroepfer, George J. Jr
, p. 1012 - 1024 (2007/10/02)
1H and 13C NMR assignments are presented for 30 oxygenated lanostane derivatives, including lanosterol, dihydrolanosterol, 7-ketolanosterol, agnosterol, 24,25-epoxylanosterol, 8α,9α-epoxylanostan-3β-ol, three 15-oxygenated derivatives of lanost-7-en-3β-ol, lanostane-3β,7α-diol, lanostane-3B,9α-diol and their acetates.These assignments, which were largely determined by a combination of DEPT, one-bond and long-range 13C-1H chemical shift correlation and lanthanide-induced shift experiments, are not dependent on previously reported assignments, several of which were found to be incorrect. 1H and 13C acetylation shifts for lanostan-3β-ols were sufficiently invariant among the sterols studied that they were useful for assigning carbons in rings A and B.The acetylation shifts reported for lanostan-3β-ols were extended and partially revised.-- Key Words 1H and 13C NMR Oxygenated lanostane derivatives Spectral assignment Lanthanide-induced shifts Long-range HECTOR Acetylation shifts
REACTION OF SOME TRISUBSTITUTED STEROID EPOXIDES WITH TRIPHENYLPHOSPHINE - IODINE DOMPLEX. DEOXYGENATION OF EPOXIDES
Paryzek, Zdzislaw,Wydra, Roman
, p. 2601 - 2604 (2007/10/02)
Triphenylphosphine - iodine complex was found to be an effective reagent for deoxygenation of trisubstituted steroidal epoxides.The mechanism of the reaction is proposed.
