Milder operating parameters for one‐step conversion of fructose to levulinic acid over sulfonated H‐β zeolite in aqueous media

Author(s):  
Swapneel K. Bisen ◽  
Prashant S. Niphadkar ◽  
Sachin U. Nandanwar ◽  
Irina Simakova ◽  
Vijay V. Bokade
2009 ◽  
Vol 2009 (29) ◽  
pp. 4926-4929 ◽  
Author(s):  
Hassan Zali Boeini ◽  
Khadijeh Hajibabaei Najafabadi
Keyword(s):  

2000 ◽  
pp. 2049-2050 ◽  
Author(s):  
Filipe Rodrigues ◽  
Yves Canac ◽  
André Lubineau
Keyword(s):  

1992 ◽  
Vol 40 (11) ◽  
pp. 2309-2314 ◽  
Author(s):  
Turlough F. Guerin ◽  
Stephen W. L. Kimber ◽  
Ivan R. Kennedy
Keyword(s):  

1999 ◽  
Vol 52 (2) ◽  
pp. 83 ◽  
Author(s):  
Christopher R. Strauss

Enabling technologies and methodologies were established and combined to afford various environmentally benign processes for laboratory-scale organic synthesis and for the production of fine chemicals, intermediates and pharmaceuticals. The technologies comprised continuous and batch microwave reactors and catalytic membranes. The methodologies included solvent-free conditions, catalysed or uncatalysed processes, the use of aqueous media at high temperature and non-extractive techniques for product isolation. Applications included Hofmann eliminations, Willgerodt and Jacobs–Gould reactions, indole transformations, aldol condensation, Rupe and Meyer–Schuster rearrangements and C–C coupling reactions (including a tandem Heck coupling–dehydrogenation). New processes for catalytic etherification, uncatalysed hydrogen transfer and a one-step arylamidation were also developed. Typical products were N-(4-hydroxyphenyl)acetamide, carvacrol, a-phenylacetamide, cinnamaldehyde, cinnamyl alcohol, acetophenone, indole, 3-hydroxy-1,2-dimethyl-4-pyridone, di(2-phenylethyl) ether, di(cyclopropylmethyl) ether, 3-methylcyclopent-2-enone and a synthetic precursor of nalidixic acid.


1971 ◽  
Vol 49 (15) ◽  
pp. 2586-2589 ◽  
Author(s):  
C. Freppel ◽  
R. Favier ◽  
J.-C. Richer ◽  
M. Zador

The stereochemistry of the diols obtained by oxidation of 3-t-butylcyclohexene by thallic sulfate indicates that the α hydroxyl group participates in the breaking of the C—T1 bond of the intermediate organothallous compound. The fact that only the trans diols are obtained indicates that an SN2 substitution of the thallium can be excluded. We suggest that the thallic oxidation in aqueous media of olefin of rigid conformation is an excellent one-step method of preparing trans diols. The formation of the trans diaxial diol upon oxidation of 4-t-butylcyclohexene tends to confirm that hypothesis.


2008 ◽  
Vol 8 (1) ◽  
pp. 420-423 ◽  
Author(s):  
Dimitrios Tasis ◽  
Konstantinos Papagelis ◽  
Dionysios Douroumis ◽  
James R. Smith ◽  
Nikolaos Bouropoulos ◽  
...  

The one-step dispersion of HiPco single-walled carbon nanotubes in aqueous media with the use of a synthetic lyso-phosphatidylcholine was studied. Solubilization occurs through wrapping of lipid molecules around the circumference of the tubes, yielding lipid monolayers on the graphitic sidewalls as evidenced by atomic force microscopy imaging and dynamic light scattering measurements. Raman spectroscopy showed that the dispersion and centrifugation process leads to an effective enrichment of the stable aqueous suspension in carbon nanostructures with smaller diameters.


2006 ◽  
Vol 36 (7) ◽  
pp. 843-847 ◽  
Author(s):  
Xicun Wang ◽  
Zhang Zhang ◽  
Zhengjun Quan ◽  
Mangang Wang ◽  
Fang Wang ◽  
...  
Keyword(s):  

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