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Recent advances in one-stage conversion of lipid-based biomass-derived oils into fuel components – aromatics and isomerized alkanes – aromatics and isomerized alkanes
Bis[diphenylphosphino]methane and its bridge-substituted analogues as chemically non-innocent ligands for H2 activationalkane derivative
A Simpe Model for the Description and Prediction of the Thermodynamic Substrate and Regioselectivities of Alkane CH Activation with Metal Complexes and prediction of the thermodynamic substrate and regioselectivities of alkane reactions with carbenes, nitrenes
A Simpe Model for the Description and Prediction of the Thermodynamic Substrate and Regioselectivities of Alkane CH Activation with Metal Complexes and prediction of the thermodynamic substrate and regioselectivities of alkane reactions with carbenes, nitrenes
Novel cage-like hexanuclear nickel(II) silsesquioxane. Synthesis, structure, and catalytic activity in oxidations with peroxides catalytic activity in activation of such small molecules as light alkanes and alcohols. Namely, oxidation
Nickel- and Rhenium-Containing Sulfated Zirconia Catalyst for Simultaneous Benzene Alkylation and Alkanes Isomerization of the latter to C7-C9 arenes by alkylation with the products of alkanes cracking. It has
been shown
The ability of sulfate-reducing bacteria of various taxonomic groups to synthesize extracellular hydrocarbons were normal or isomeric alkanes with a chain length from C11 to C24.
The ability of sulfate-reducing bacteria of various taxonomic groups to synthesize extracellular hydrocarbons were normal or isomeric alkanes with a chain length from C11 to C24. © 1997 MAHK Hayka
The ability of sulfate-reducing bacteria of various taxonomic groups to synthesize extracellular hydrocarbons were normal or isomeric alkanes with a chain length from C11 to C24.
The ability of sulfate-reducing bacteria of various taxonomic groups to synthesize extracellular hydrocarbons were normal or isomeric alkanes with a chain length from C11 to C24. © 1997 MAHK Hayka
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