Synthesis of triaromatic steroid hydrocarbons methylated at position 2, 3 or 6: molecular fossils of yet unknown biological origin

Eric Lichtfouse; Pierre Albrecht

doi:10.1016/S0040-4020(01)80848-6

Synthesis of triaromatic steroid hydrocarbons methylated at position 2, 3 or 6: molecular fossils of yet unknown biological origin

Eric Lichtfouse
, Pierre Albrecht

科研成果: 期刊稿件 › 文章 › 同行评审

17 引用（Scopus）

摘要

C_21-29 triaromatic steroid hydrocarbons bearing a methyl group at unusual positions 2, 3 or 6 have been synthesized from pregnenolone, cholesterol or stigmasterol via stera-3,5-dienes. Their occurrence in various sedimentary rocks and petroleums suggests the presence of yet unknown biological precursors.

源语言	英语
页（从-至）	1731-1744
页数	14
期刊	Tetrahedron
卷	50
期	6
DOI	https://doi.org/10.1016/S0040-4020(01)80848-6
出版状态	已出版 - 7 1月 1994
已对外发布	是

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abstract = "C21-29 triaromatic steroid hydrocarbons bearing a methyl group at unusual positions 2, 3 or 6 have been synthesized from pregnenolone, cholesterol or stigmasterol via stera-3,5-dienes. Their occurrence in various sedimentary rocks and petroleums suggests the presence of yet unknown biological precursors.",

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AB - C21-29 triaromatic steroid hydrocarbons bearing a methyl group at unusual positions 2, 3 or 6 have been synthesized from pregnenolone, cholesterol or stigmasterol via stera-3,5-dienes. Their occurrence in various sedimentary rocks and petroleums suggests the presence of yet unknown biological precursors.

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DO - 10.1016/S0040-4020(01)80848-6

M3 - 文章

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Synthesis of triaromatic steroid hydrocarbons methylated at position 2, 3 or 6: molecular fossils of yet unknown biological origin

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