Relevant bibliographies by topics / Pentanetriol

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  1. Journal articles

Academic literature on the topic 'Pentanetriol'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Pentanetriol"

1

Zhu, Chun, Travis B. Meador, Wolf Dummann, and Kai-Uwe Hinrichs. "Identification of unusual butanetriol dialkyl glycerol tetraether and pentanetriol dialkyl glycerol tetraether lipids in marine sediments." Rapid Communications in Mass Spectrometry 28 (December 27, 2013): 332–38. https://doi.org/10.1002/rcm.6792.

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RATIONALE: Glycerol serves as the principal backbone moiety bound to various acyl/alkyl chains for membrane lipids of <em>Eukarya</em>, <em>Bacteria</em>, and <em>Archaea</em>. In this study, we report a suite of unusual tetraether lipids in which one of the two conventional glycerol backbones is substituted by butanetriol or pentanetriol. METHODS: Identification of these lipids was achieved via diagnostic fragments and their expected acetylation products using liquid chromatography/mass spectrometry (LC/MS), and their diagnostic ether cleavage products using gas chromatography/mass spectromet
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2

Coffinet, Sarah, Travis B. Meador, Lukas Mühlena, et al. "Structural elucidation and environmental distributions of butanetriol and pentanetriol dialkyl glycerol tetraethers (BDGTs and PDGTs)." Biogeosciences 17, no. 2 (2020): 317–30. http://dx.doi.org/10.5194/bg-17-317-2020.

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Abstract. Butanetriol and pentanetriol dialkyl glycerol tetraethers (BDGTs and PDGTs) are membrane lipids, recently discovered in sedimentary environments and in the methanogenic archaeon Methanomassiliicoccus luminyensis. They possess an unusual structure, which challenges fundamental assumptions in lipid biochemistry. Indeed, they bear a butanetriol or a pentanetriol backbone instead of a glycerol at one end of their core structure. In this study, we unambiguously located the additional methyl group of the BDGT compound on the C3 carbon of the lipid backbone via high-field nuclear magnetic r
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3

Chênevert, Robert, and Gabriel Courchesne. "Enzymatic desymmetrization of meso(anti-anti)-2,4-dimethyl-1,3,5-pentanetriol." Tetrahedron: Asymmetry 6, no. 9 (1995): 2093–96. http://dx.doi.org/10.1016/0957-4166(95)00272-q.

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4

FEDORTSOVA, E. V., G. S. IDLIS, E. M. SHVARTS, and A. Z. KAMARS. "ChemInform Abstract: Reaction of Boric Acid with 3-Methyl-1,3,5-pentanetriol." ChemInform 26, no. 21 (2010): no. http://dx.doi.org/10.1002/chin.199521177.

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5

Santaniello, Enzo, Rosangela Casati, Lucio Ceriani, Patrizia Ferraboschi, and Paride Grisenti. "Synthesis of 3-methyl-1,3,5-pentanetriol and its mono- and diesters." Chemistry and Physics of Lipids 49, no. 1-2 (1988): 97–100. http://dx.doi.org/10.1016/0009-3084(88)90069-2.

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6

CHENEVERT, R., and G. COURCHESNE. "ChemInform Abstract: Enzymatic Desymmetrization of meso(anti-anti)-2,4-Dimethyl-1,3,5- pentanetriol." ChemInform 27, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199606069.

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7

Becker, Kevin W., Felix J. Elling, Marcos Y. Yoshinaga, Andrea Söllinger, Tim Urich, and Kai-Uwe Hinrichs. "Unusual Butane- and Pentanetriol-Based Tetraether Lipids in Methanomassiliicoccus luminyensis, a Representative of the Seventh Order of Methanogens." Applied and Environmental Microbiology 82, no. 15 (2016): 4505–16. http://dx.doi.org/10.1128/aem.00772-16.

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ABSTRACTA new clade of archaea has recently been proposed to constitute the seventh methanogenic order, theMethanomassiliicoccales, which is related to theThermoplasmatalesand the uncultivated archaeal clades deep-sea hydrothermal ventEuryarchaeotagroup 2 and marine group IIEuryarchaeotabut only distantly related to other methanogens. In this study, we investigated the membrane lipid composition ofMethanomassiliicoccus luminyensis, the sole cultured representative of this seventh order. The lipid inventory ofM. luminyensiscomprises a unique assemblage of novel lipids as well as lipids otherwis
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8

Yusufo??lu, Ayşe, Stefan Antons, and Hans-Dieter Scharf. "Syntheses of pure enantiomers oferythro-1,2,3-pentanetriol and their 1-Bromo- and 1-Tosyloxy Derivatives." Liebigs Annalen der Chemie 1986, no. 6 (1986): 1119–23. http://dx.doi.org/10.1002/jlac.198619860616.

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9

MacQueen, Blake, Michael Royko, Bradie S. Crandall, Andreas Heyden, Yomaira J. Pagán-Torres, and Jochen Lauterbach. "Kinetics Study of the Hydrodeoxygenation of Xylitol over a ReOx-Pd/CeO2 Catalyst." Catalysts 11, no. 1 (2021): 108. http://dx.doi.org/10.3390/catal11010108.

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In this study, we elucidate the reaction kinetics for the simultaneous hydrodeoxygenation of xylitol to 1,2-dideoxypentitol and 1,2,5-pentanetriol over a ReOx-Pd/CeO2 (2.0 weight% Re, 0.30 weight% Pd) catalyst. The reaction was determined to be a zero-order reaction with respect to xylitol. The activation energy was elucidated through an Arrhenius relationship as well as non-Arrhenius kinetics. The Arrhenius relationship was investigated at 150–170 °C and a constant H2 pressure of 10 bar resulting in an activation energy of 48.7 ± 10.5 kJ/mol. The investigation of non-Arrhenius kinetics was co
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10

Zhu, Chun, Travis B. Meador, Wolf Dummann, and Kai-Uwe Hinrichs. "Identification of unusual butanetriol dialkyl glycerol tetraether and pentanetriol dialkyl glycerol tetraether lipids in marine sediments." Rapid Communications in Mass Spectrometry 28, no. 4 (2013): 332–38. http://dx.doi.org/10.1002/rcm.6792.

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