Sterols of a diatomaceous ooze from Walvis Bay.
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Africa, Eastern↗
Biomedical subjects
J R Maxwell
Publications and source records attributed to J R Maxwell.
Monocarboxylic acids from oxidation of acyclic isoprenoid alkanes by Mycobacterium fortuitum.
Mycobacterium fortuitum utilizes certain stereoisometric mixtures of individual multimethyl branched alkanes as sole carbon source, including 2,6(R), 10(S), 14(RS)-tetramethylhexadecane; 2.6(R), 10(S), 14(RS)-tetramethylheptadecane; 2,6(RS), 10(RS)-trimethyltetradecane, and 2,6(R), 10(S)-trimethylpentadecane. Products of oxidation isolated from the bacterial lipids were acids derived predominantly from oxidation of the isopropyl terminus of each alkane, except in the case of 2,6(RS), 10(RS)-trimethyltetradecane. With the latter, acids from oxidation at either terminus were detected in comparable proportions.
Alkanes↗
Stereochemical studies of acyclic isoprenoid compounds. IV. Microbial oxidation of 2,6,10,14-tetramethylpentadecane (pristane).
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Chemistry, Organic↗
Carbon chemistry of the Apollo lunar samples.
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Amino Acids↗
Lunar carbon chemistry: relations to and implications for terrestrial organic geochemistry.
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Astronomical Phenomena↗
Stereochemical studies of acyclic isoprenoid compounds. 3. The stereochemistry of naturally occurring (marine) 2,6,10,14-tetramethylpentadecane.
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Alkanes↗
Carbon chemistry of the lunar surface.
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News↗
Indigenous lunar methane and ethane.
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Journal Article↗