Journal of Organic Chemistry p. 4493 - 4497 (1983)
Update date:2022-08-02
Topics: Synthesis Mass spectrometry Isomer Chemical Synthesis Gas Chromatography Hydrocarbon Steroid
Bauer, Philip E.
Dunlap, Norma K.
Arseniyadis, Simeon
Watt, David S.
Seifert, Wolfgang K.
Moldowan, J. Michael
21-Hydroxyhopan-3-one was converted to a mixture of 22,29,30-trinor-17α-hopan-21-one and 30-norhopan-22-one by the following reaction sequence: (1) dehydration with phosphorus oxytrichloride, (2) Wolff-Kishner reduction, and (3) ozonolysis.These two keton
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Doi:10.1016/j.tetlet.2020.152584
(2020)Doi:10.1016/S0040-4020(01)00274-5
(2001)Doi:10.1246/bcsj.53.3035
(1980)Doi:10.1246/bcsj.52.1911
(1979)Doi:10.1016/0045-2068(75)90046-2
(1975)Doi:10.1007/BF00862179
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