Search results for "carbon"

Thermal rearrangements of 1,2-dialkoxybenzenes by flash vacuum pyrolysis

1995

Flash vacuum pyrolysis of 1,2-dialkoxybenzenes 1a-c leads to the liberation of alkanes from the interacting side chains. A rearrangement of the skeleton yields the o-hydroxy carbonyl compounds 2 and 4. The generation of phenol 3 can be rationalized by a decarbonylation. The latter reaction is the sole process which can be observed for the bicyclic starting compound 9.

Carbon Dioxide as Chemical Feedstock. Edited by Michele Aresta.

2010

Topical Anti-Inflammatory Lignans from Haplophyllum hispanicum Haplophyllum hispanicum

1996

The present paper reports the results of the methanol extract of Haplophyllum hispanicum Spach on single or repeated local 12-O-tetradecanoylphorbol acetate (TPA) administration and in the oxazolone-induced contact-delayed hypersensitivity mouse ear edemas. Two topical anti-inflammatory aryl naphthalide lignans were isolated from the active fractions of the methanol extract. They were identified by spectroscopic methods, including 13C NMR and heteronuclear multiple bond correlation (HMBC), as diphyllin acetyl apioside and tuberculatin. The former was the most active on acute TPA edema with a ID50 of 0.27 μmol/ear

ChemInform Abstract: Imidazolium and Potassium Hydrogen Carbonate Salts as Ecofriendly Organocatalysts for Oxazolidinone Synthesis.

2016

Although oxazolidinones are valuable intermediate compounds for industrial applications, no synthetic method is suitable for their production on a large scale owing to the use of reagents/catalysts that are hazardous or toxic to human health or ecotoxic for the environment. In this manuscript, we describe new and efficient catalysts, that is, the nontoxic hydrogen carbonate anion in combination with a potassium or diisobutylimidazolium ([iBu(2)IM]) countercation, for the conversion of -amino alcohols into cyclic oxazolidinones in high yields of 69 to 90%. Depending on the catalytic conditions, both catalysts could be easily recovered from the crude reaction products and reused several times…

ChemInform Abstract: Cyclocondensation of 6-Acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine with Hydroxylamine and Hydrazine.

2010

The cyclocondensation of 6-acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine (3) with hydroxylamine or hydrazine leads to 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenylisoxazolo-[5,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4a) and 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenyl-1H-pyrazolo[3,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4b), respectively. In the presence of methanolic hydrogen chloride, 4b undergoes a cleavage of the pyrimidine ring to yield (5-amino-1,2,4-triazol-1-yl)(3,5-dimethylpyrazol-4-yl)phenylmethane (5). The structure determination of the compounds obtained is based on 1H and 13C nmr spectra including NOE measurements.

Cyclocondensation of 6-acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine with hydroxylamine and hydrazine

1998

The cyclocondensation of 6-acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine (3) with hydroxylamine or hydrazine leads to 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenylisoxazolo-[5,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4a) and 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenyl-1H-pyrazolo[3,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4b), respectively. In the presence of methanolic hydrogen chloride, 4b undergoes a cleavage of the pyrimidine ring to yield (5-amino-1,2,4-triazol-1-yl)(3,5-dimethylpyrazol-4-yl)phenylmethane (5). The structure determination of the compounds obtained is based on 1H and 13C nmr spectra including NOE measurements.

Recent Scientific and Technological Developments in Electrochemical Carboxylation Based on Carbon Dioxide

2010

Biotrickling Filters for Removal of Volatile Organic Compounds from Air in the Coating Sector

2013

Self-Assembled DNA-Based Structures for Nanoelectronics

2023

Recent developments in structural DNA nanotechnology have made com-plex and spatially exactly controlled self-assembled DNA nanoarchitectureswidely accessible. The available methods enable large variety of differ-ent possible shapes combined with the possibility of using DNA structuresas templates for high-resolution patterning of nano-objects, thus openingup various opportunities for diverse nanotechnological applications. TheseDNA motifs possess enormous possibilities to be exploited in realization ofmolecular scale sensors and electronic devices, and thus, could enable fur-ther miniaturization of electronics. However, there are arguably two mainissues on making use of DNA-based electroni…

Nanocomposite, an innovative route to large structure and infrastructure protection. A case of study: CNT-doped polyurea

2010

<p>In this work we focus on experimental studies of polymer-nanocomposites intended for passive protection of civil structures. The material consists of a polyurea-matrix enhanced by different quantities of multiwalled carbon nanotubes. Several tensile and cyclic tests are performed to evaluate and characterize the mechanical behaviour of this new material. Furthermore, we subject the material to accelerated thermal aging and study its performance deterioration which is fairly unknown. The results on the unaged specimens are intuitive and indicate that an arbitrary amount of CNTs may result in suboptimal performance. More specifically, 1% in weight of CNTs yields the best mechanical p…