Results 261 to 270 of about 67,475 (292)
Allosteric Ensembles Elucidate Mechanisms of Inhibition in Human Soluble Epoxide Hydrolase
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Journal of the American Chemical Society, 2021
Selective hydrogenation of epoxides would be a direct and powerful approach for alcohol synthesis, but it has proven to be elusive. Here, electrochemically epoxide hydrogenation using electrons and protons as reductants is reported. A wide range of primary, secondary, and tertiary alcohols can be achieved through selective Markovnikov or anti ...
Cheng Huang +5 more
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Selective hydrogenation of epoxides would be a direct and powerful approach for alcohol synthesis, but it has proven to be elusive. Here, electrochemically epoxide hydrogenation using electrons and protons as reductants is reported. A wide range of primary, secondary, and tertiary alcohols can be achieved through selective Markovnikov or anti ...
Cheng Huang +5 more
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Journal of the American Chemical Society, 2008
Oxidation of graphite may be carried out by reaction with meta-chloroperoxybenzoic acid to yield graphite epoxide. Scanning tunneling microscopy (STM) showed that the functionalization occurs at the edges rather than on the basal plane of the graphite.
Jayanta, Chattopadhyay +8 more
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Oxidation of graphite may be carried out by reaction with meta-chloroperoxybenzoic acid to yield graphite epoxide. Scanning tunneling microscopy (STM) showed that the functionalization occurs at the edges rather than on the basal plane of the graphite.
Jayanta, Chattopadhyay +8 more
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Chemistry and Physics of Lipids, 2001
Previously unknown 4,5-epoxy-N-acetyl-sphingosine (1) was synthesized by epoxidation of N-acetyl-sphingosine with 1,1-dimethyldioxirane. A by-product generated by HPLC purification is the tetrahydrofuryl derivative of acetamide (2). Mainly allylic oxidation was observed when natural ceramides were reacted with dimethyldioxirane.
A, Möllenberg, G, Spiteller
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Previously unknown 4,5-epoxy-N-acetyl-sphingosine (1) was synthesized by epoxidation of N-acetyl-sphingosine with 1,1-dimethyldioxirane. A by-product generated by HPLC purification is the tetrahydrofuryl derivative of acetamide (2). Mainly allylic oxidation was observed when natural ceramides were reacted with dimethyldioxirane.
A, Möllenberg, G, Spiteller
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Proceedings of the 2015 ACM Conference on Special Interest Group on Data Communication, 2015
SDN opens a new chapter in network troubleshooting as besides misconfigurations and firmware/hardware errors, software bugs can occur all over the SDN stack. As an answer to this challenge the networking community developed a wealth of piecemeal SDN troubleshooting tools aiming to track down misconfigurations or bugs of a specific nature (e.g.
Tamás Lévai +3 more
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SDN opens a new chapter in network troubleshooting as besides misconfigurations and firmware/hardware errors, software bugs can occur all over the SDN stack. As an answer to this challenge the networking community developed a wealth of piecemeal SDN troubleshooting tools aiming to track down misconfigurations or bugs of a specific nature (e.g.
Tamás Lévai +3 more
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ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
R. A. Sheldon, M. C. A. Van Vliet
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AbstractFor Abstract see ChemInform Abstract in Full Text.
R. A. Sheldon, M. C. A. Van Vliet
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Epoxidations: Titanium‐Catalyzed Epoxidation
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
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Chemico-Biological Interactions, 1988
Epoxide hydrolase activity is recovered in the high-speed supernatant fraction from the liver of all mammals so far examined, including man. For some as yet unexplained reason, the rat has a very low level of this activity, so that cytosolic epoxide hydrolase is generally studied in mice.
J, Meijer, J W, DePierre
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Epoxide hydrolase activity is recovered in the high-speed supernatant fraction from the liver of all mammals so far examined, including man. For some as yet unexplained reason, the rat has a very low level of this activity, so that cytosolic epoxide hydrolase is generally studied in mice.
J, Meijer, J W, DePierre
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Aliphatic Epoxide Carboxylation
Annual Review of Biochemistry, 2003▪ Abstract Aliphatic epoxides (epoxyalkanes) are highly reactive electrophilic molecules that are formed from the monooxygenase-catalyzed epoxidation of aliphatic alkenes. The bacterial metabolism of short-chain epoxyalkanes occurs by a three-step pathway resulting in net carboxylation to β-ketoacids.
Scott A, Ensign, Jeffrey R, Allen
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