78 research outputs found
Catalytic Intermolecular Hetero-Dehydro-DielsâAlder Cycloadditions: Regio- and Diasteroselective Synthesis of 5,6-Dihydropyridin-2-ones
A novel catalyzed intermolecular heterodehydro-DielsâAlder reaction between pushâpull 1,3-dien-5-ynes and aldimines or silylaldimines is reported. The sequence is promoted both by gold(I) or silver(I) catalysts and leads to the diastereo- and regioselective formation of 5,6-dihydropyridin-2-onesMICINN (Spain) (grants CTQ2009-09949, CTQ2010-16790, PTA2008-1524-P contract to J.M.F.-G. and Ramon y Cajal postdoctoral contract to M.A.F.-R.) and FICYT (project IB08-088)This document is the Accepted Manuscript version of a Published Work that appeared in final form in
Organic letters, copyright © American Chemical Society after peer review and technical editing by the publisher.
To access the final edited and published work see http://pubs.acs.org/page/policy/articlesonrequest/index.htm
A Randomized, Double Blind, Placebo-Controlled Trial of Pioglitazone in Combination with Riluzole in Amyotrophic Lateral Sclerosis
BACKGROUND: Pioglitazone, an oral anti-diabetic that stimulates the PPAR-gamma transcription factor, increased survival of mice with amyotrophic lateral sclerosis (ALS).
METHODS/PRINCIPAL FINDINGS: We performed a phase II, double blind, multicentre, placebo controlled trial of pioglitazone in ALS patients under riluzole. 219 patients were randomly assigned to receive 45 mg/day of pioglitazone or placebo (one: one allocation ratio). The primary endpoint was survival. Secondary endpoints included incidence of non-invasive ventilation and tracheotomy, and slopes of ALS-FRS, slow vital capacity, and quality of life as assessed using EUROQoL EQ-5D. The study was conducted under a two-stage group sequential test, allowing to stop for futility or superiority after interim analysis. Shortly after interim analysis, 30 patients under pioglitazone and 24 patients under placebo had died. The trial was stopped for futility; the hazard ratio for primary endpoint was 1.21 (95% CI: 0.71-2.07, pâ=â0.48). Secondary endpoints were not modified by pioglitazone treatment. Pioglitazone was well tolerated.
CONCLUSION/SIGNIFICANCE: Pioglitazone has no beneficial effects on the survival of ALS patients as add-on therapy to riluzole.
TRIAL REGISTRATION: Clinicaltrials.gov NCT00690118
Gold(I)-Catalyzed Coupling Reactions for the Synthesis of Diverse Small Molecules Using the Build/Couple/Pair Strategy
The build/couple/pair strategy has yielded small molecules with stereochemical and skeletal diversity by using short reaction sequences. Subsequent screening has shown that these compounds can achieve biological tasks considered challenging if not impossible (âundruggableâ) for small molecules. We have developed gold(I)-catalyzed cascade reactions of easily prepared propargyl propiolates as a means to achieve effective intermolecular coupling reactions for this strategy. Sequential alkyne activation of propargyl propiolates by a cationic gold(I) catalyst yields an oxocarbenium ion that we previously showed is trapped by C-based nucleophiles at an extrannular site to yield α-pyrones. Here, we report O-based nucleophiles react by ring opening to afford a novel polyfunctional product. In addition, by coupling suitable building blocks, we subsequently performed intramolecular pairing reactions that yield diverse and complex skeletons. These pairing reactions include one based on a novel aza-Wittig-6Ï-electrocyclization sequence and others based on ring-closing metathesis reactions.Chemistry and Chemical Biolog
Stereoselective synthesis of cyclopropanes based on a 1,2-chirality transfer
A stereoselective route to enantiomerically enriched bicyclic cyclopropane derivatives 13 is described which is based on a conceptually novel 1,2-chirality transfer approach. The hyperconjugative interaction of an electronically excited carbonyl group with the * orbital of an adjacent C-X bond in the transition state of a hydrogen abstraction causes the preference of a certain conformation and consequently the differentiation between two diastereotopic methylene groups. The 1,2-chirality transfer is completed by a subsequent HX elimination which destroys the only stereogenic center in the reactants 12. Furthermore, it was found that contrary enthalpic and entropic influences result in the existence of an inversion temperature T0. Upon crossing T0 the stereoselectivity is reversed. Considering this temperature dependency, chirality transfer efficiencies of up to 83% could be achieved. The absolute configuration of most products could be unambiguously determined by VCD sp ectroscopy combined with DFT calculations
Photochemical Reactions of Nitroso Oxides at Low Temperatures:Â The First Experimental Evidence for Dioxaziridines
Carbon nanodots revised : the thermal citric acid/urea reaction
Luminescent compounds obtained from the thermal reaction of citric acid and urea have been studied and utilized in different applications in the past few years. The identified reaction products range from carbon nitrides over graphitic carbon to distinct molecular fluorophores. On the other hand, the solid, non-fluorescent reaction product produced at higher temperatures has been found to be a valuable precursor for the CO2-laser-assisted carbonization reaction in carbon laser-patterning. This work addresses the question of structural identification of both, the fluorescent and non-fluorescent, reaction products obtained in the thermal reaction of citric acid and urea. The reaction products during autoclave-microwave reactions in the melt were thoroughly investigated in dependence of the reaction temperature and the reaction products were subsequently separated by a series of solvent extractions and column chromatography. The evolution of a green molecular fluorophore, namely HPPT, was confirmed and a full characterization on its structure and photophysical properties was conducted. The additional blue fluorescence is attributed to oligomeric ureas, which was confirmed by complementary optical and structural characterization. These two components form strong hydrogen-bond networks which eventually react to form solid, semi-crystalline particles with sizes ~7 nm and an elemental composition of 46% C, 22% N, and 29% O. The structural features and properties of all three main components were investigated in a comprehensive characterization study
Molecular Rods Based on Oligo-spiro-thioketals
We report on an extension of the
previously established concept
of oligospiroketal (OSK) rods by replacing a part or all ketal moieties
by thioketals leading to oligospirothioketal (OSTK) rods. In this
way, some crucial problems arising from the reversible formation of
ketals are circumvented. Furthermore, the stability of the rods toward
hydrolysis is considerably improved. To successfully implement this
concept, we first developed a number of new oligothiol building blocks
and improved the synthetic accessibility of known oligothiols, respectively.
Another advantage of thioacetals is that terephthalaldehyde (TAA)
sleeves, which are too flexible in the case of acetals can be used
in OSTK rods. The viability of the OSTK approach was demonstrated
by the successful preparation of some OSTK rods with a length of some
nanometers
Molecular Rods Based on Oligo-spiro-thioketals
We report on an extension of the
previously established concept
of oligospiroketal (OSK) rods by replacing a part or all ketal moieties
by thioketals leading to oligospirothioketal (OSTK) rods. In this
way, some crucial problems arising from the reversible formation of
ketals are circumvented. Furthermore, the stability of the rods toward
hydrolysis is considerably improved. To successfully implement this
concept, we first developed a number of new oligothiol building blocks
and improved the synthetic accessibility of known oligothiols, respectively.
Another advantage of thioacetals is that terephthalaldehyde (TAA)
sleeves, which are too flexible in the case of acetals can be used
in OSTK rods. The viability of the OSTK approach was demonstrated
by the successful preparation of some OSTK rods with a length of some
nanometers
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