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首页> 外文期刊>European journal of organic chemistry >Identification of a fossil sterane biomarker in crude oil - An androstane with a modified carbon skeleton
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Identification of a fossil sterane biomarker in crude oil - An androstane with a modified carbon skeleton

机译:原油中化石甾烷生物标志物的鉴定-具有修饰碳骨架的雄烷

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Three constitutional isomers of androstane were prepared for comparison with three unknown fossil C_(19)H_(32) organic biomarkers ("19A", "19B", and "19C" in elution order in geological samples from Oman. 3β-Methyl-A-nor-androstane was prepared in six steps (8 % overall yield from testosterone. The key steps of this sequence were an Eschenmoser fragmentation and recyclization of the A ring. A mixture of four stereoisomers of 3-methyl-A-nor-androstane (4 % overall yield was prepared by ionic hydrogenation of the olefin after A-ring recyclization in three steps. 17-Methyl-18-nor-androstane was synthesized in four steps as a mixture of isomers (58 % overall yield from dihydrotestosterone with a Wagner-Meerwein shift of the 13β-methyl group to C-17 as the key step. Pure 17β- and 17α-methyl-18-nor-13α-androstane (4 and 2 % overall yield, respectively were obtained in three additional steps after α-oxidation of the Wagner-Meerwein rearrangement product and subsequent reduction. The synthesis of 18-nor-D-homo-13β-androstane (12 % yield over seven steps from dihydrotestosterone involved oxidative cleavage of the C-C double bond in the Wagner-Meerwein rearrangement product from the previous synthesis and subsequent recyclization of the D ring followed by reduction. The relative configurations of all final products were confirmed by X-ray crystallography. A comparison of the synthetic standards with the saturated hydrocarbon fraction of an Oman crude oil by gas chromatography (GC-MS coinjection on three different GC columns and comparison of mass spectra revealed that unknown compound 19C is 18-nor-D-homo-13β,14α-androstane, whereas the isomeric 3-methyl-A-nor-androstanes and 17-methyl-18-nor-androstanes elute close to 19A and 19B, respectively, but do not match the unknowns. New old fossil: The so far unknown constitution of a fossil sterane biomarker in crude oil from Oman was elucidated to be 18-nor-D-homo-androstane by comparison with a synthetic reference compound.
机译:制备了雄烷三烷的三种结构异构体,用于与阿曼地质样品中的三种未知化石C_(19)H_(32)有机生物标记物(“ 19A”,“ 19B”和“ 19C”)进行洗脱比较。3β-甲基-A -nor-androstane分六个步骤制备(睾丸激素的总产率为8%。此序列的关键步骤是Eschenmoser片段化和A环的再循环。3-甲基-A-nor-androstane的四种立体异构体的混合物(分三步进行A环再循环后,通过烯烃的离子加氢反应可制得4%的总收率。分四个步骤以异构体混合物的形式合成了17-甲基-18-正雄烷酮(58%的二氢睾丸激素和Wagner收率) -关键的步骤是将13β-甲基的Meerwein转变为C-17。纯净的17β-和17α-甲基-18-nor-13α-雄甾烷(分别在α后的三个附加步骤中分别获得了4%和2%的总收率) -Wagner-Meerwein重排产物的-氧化和随后的还原。 18-nor-D-homo-13β-雄烷酮的合成(二氢睾丸酮在七个步骤中的12%收率涉及先前合成中Wagner-Meerwein重排产物中CC双键的氧化裂解,随后D环的再环化,然后还原。所有最终产物的相对构型通过X射线晶体学证实。通过气相色谱法(在三个不同的GC柱上进行GC-MS共注入)对合成标准品与阿曼原油的饱和烃馏分进行比较,并进行质谱比较,结果表明未知化合物19C为18-nor-D-homo-13β, 14α-雄烷烷,而异构的3-甲基-A-正雄烷和17-甲基-18-正雄烷分别洗脱至19A和19B,但与未知物不符新的旧化石:迄今未知与合成参考化合物相比,阿曼原油中化石甾烷生物标志物的组成被阐明为18-nor-D-homo-androstane。

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