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

Research output: Contribution to journal › Article › peer-review

17 Scopus citations

Abstract

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.

Original language	English
Pages (from-to)	1731-1744
Number of pages	14
Journal	Tetrahedron
Volume	50
Issue number	6
DOIs	https://doi.org/10.1016/S0040-4020(01)80848-6
State	Published - 7 Jan 1994
Externally published	Yes

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

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.",

author = "Eric Lichtfouse and Pierre Albrecht",

year = "1994",

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doi = "10.1016/S0040-4020(01)80848-6",

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T1 - Synthesis of triaromatic steroid hydrocarbons methylated at position 2, 3 or 6

T2 - molecular fossils of yet unknown biological origin

AU - Lichtfouse, Eric

AU - Albrecht, Pierre

PY - 1994/1/7

Y1 - 1994/1/7

N2 - 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.

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.

UR - https://www.scopus.com/pages/publications/0028355339

U2 - 10.1016/S0040-4020(01)80848-6

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

M3 - 文章

AN - SCOPUS:0028355339

SN - 0040-4020

VL - 50

SP - 1731

EP - 1744

JO - Tetrahedron

JF - Tetrahedron

IS - 6

ER -

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

Abstract

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