1989
DOI: 10.1016/0016-7037(89)90034-3
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Limited double bond isomerisation and selective hydrogenation of sterenes during early diagenesis

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Cited by 109 publications
(23 citation statements)
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“…Under general geologic conditions, all kinds of sterenes were converted into saturated steranes through hydrogenation (for example, sterene→sterane, diasterene→diasterane, 4-methyl diasterene→4-methyl diasterane) (de Leeuw et al, 1989). The extensive occurrence of hydrogenation indicates that the olefinic bond was easily hydrogenated and reduced.…”
Section: Formation Pathway Of Sulfur-containing Steroids and The Hydrmentioning
confidence: 99%
“…Under general geologic conditions, all kinds of sterenes were converted into saturated steranes through hydrogenation (for example, sterene→sterane, diasterene→diasterane, 4-methyl diasterene→4-methyl diasterane) (de Leeuw et al, 1989). The extensive occurrence of hydrogenation indicates that the olefinic bond was easily hydrogenated and reduced.…”
Section: Formation Pathway Of Sulfur-containing Steroids and The Hydrmentioning
confidence: 99%
“…**-stenols (XI) to A3,5,22 -steratrienes, hydrogenation to A'. *'-steradienes, and subsequent isomerization (DE LEEUW et al, 1989). Some of these processes may be microbially mediated (WAKEHAM, 1987).…”
Section: Unsaturated Steroid Hydrocarbonsmentioning
confidence: 99%
“…A great number of studies have reported that hopanes and steranes also can be released from kerogen and/or solid bitumen by thermal pyrolysis, chemical degradation and catalytic hydropyrolysis (Seifert, 1978;Tissot and Welte, 1978;Mackenzie et al, 1982aMackenzie et al, , 1982bMycke and Michaelis, 1986;Eglinton and Douglas, 1987;Mycke et al, 1987;de Leeuw et al, 1989;Abbott et al, 1990;Hoffman et al, 1992;Richnow et al, 1992;Adam et al, 1993;Love et al, 1995;Muhammad and Abbott, 2012). Various conditions (temperature and time) have been used for thermal pyrolysis.…”
Section: Introductionmentioning
confidence: 99%