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1.
ChemSusChem ; 7(9): 2742-7, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25088205

RESUMEN

The synthesis of furoins from biomass-derived furfural and 2-methylfurfural is demonstrated in high yields in green and renewable solvents using N-heterocyclic carbene organocatalysts. The resulting furoin molecules are used as precursors for fuels using cascade catalysis, first by using Pd/C with acidic co-catalysts under very mild conditions to yield oxygenated C12 molecules. Two main products were formed, which we identified as 1,2-bis(5-methyltetrahydrofuran-2-yl)ethane and 1-(5-methyltetrahydrofuran-2-yl)heptanol. The use of a Pd/Zeolite-ß catalyst under more extreme conditions resulted in the complete hydrodeoxygenation of 5,5'-dimethylfuroin to dodecanes in high yields (76%) and exceptional selectivity (94%) for n-dodecane.


Asunto(s)
Furaldehído/química , Furaldehído/síntesis química , Oxígeno/química , Biomasa , Catálisis , Técnicas de Química Sintética , Metano/análogos & derivados , Metano/química , Paladio/química , Petróleo
2.
Inorg Chem ; 49(11): 4741-3, 2010 Jun 07.
Artículo en Inglés | MEDLINE | ID: mdl-20441158

RESUMEN

Low catalyst loading of a cationic oxorhenium(V) oxazoline complex, [2-(2'-hydroxyphenyl)-2-oxazolinato(-2)]oxorhenium(v), condenses diols and aldehydes to give 1,3-dioxolanes in excellent yields under neat conditions and reasonably mild temperatures. The reaction is applicable to biomass-derived furfural and glycerol. The resulting cyclic acetals may find use as value-added chemicals and/or oxygenate fuel additives. Differences in the stereoselectivity of the reaction for epoxides versus diols provide insight into the reaction mechanism.


Asunto(s)
Dioxanos/síntesis química , Dioxolanos/síntesis química , Furaldehído/química , Glicerol/química , Compuestos Organometálicos/química , Catálisis , Dioxanos/química , Dioxolanos/química , Estructura Molecular , Oxazoles/química , Oxígeno/química , Renio/química , Estereoisomerismo
3.
Proc Natl Acad Sci U S A ; 105(6): 2226-31, 2008 Feb 12.
Artículo en Inglés | MEDLINE | ID: mdl-18256186

RESUMEN

Cytokinesis partitions the cell by a cleavage furrow in animals but by a new cross wall in plants. How this new wall assembles at the molecular level and connects with the mother cell wall remains unclear. A lethal Arabidopsis embryogenesis mutant designated root-, shoot-, hypocotyl-defective (rsh) provides some clues: RSH encodes extensin AtEXT3, a structural glycoprotein located in the nascent cross wall or "cell plate" and also in mature cell walls. Here we report that electron micrographs of rsh mutant cells lacking RSH extensin correspond to a wall phenotype typified by incomplete cross wall assembly. Biochemical characterization of the purified RSH glycoprotein isolated from wild-type Arabidopsis cell cultures confirmed its identity as AtEXT3: a (hydroxy)proline-rich glyco protein comprising 11 identical amphiphilic peptide repeats with a 28-residue periodicity: SOOOOKKHYVYKSOOOOVKHYSOOOVYH (O = Hyp), each repeat containing a hydrophobic isodityrosine cross-link motif (YVY, underlined). Atomic force microscopy of RSH glycoprotein imaged its propensity for self-assembly into a dendritic scaffold. Extensin peroxidase catalyzed in vitro formation of insoluble RSH gels with concomitant tyrosine cross-linking, hence this likelihood in muro. We conclude that self-assembling amphiphiles of lysine-rich RSH extensin form positively charged scaffolds in the cell plate. These react with negatively charged pectin to create an extensin pectate coacervate that may template further orderly deposition of the new cross wall at cytokinesis.


Asunto(s)
Arabidopsis/citología , Pared Celular/ultraestructura , Glicoproteínas/fisiología , Proteínas de Plantas/fisiología , Secuencia de Aminoácidos , Glicoproteínas/química , Microscopía de Fuerza Atómica , Microscopía Electrónica de Transmisión , Datos de Secuencia Molecular , Proteínas de Plantas/química
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