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111.
Friedemann Leipold Florian Rudroff Marko D. Mihovilovic Uwe T. Bornscheuer 《Tetrahedron: Asymmetry》2013,24(24):1620-1624
The substrate scope of a steroid monooxygenase (STMO) from Rhodococcus rhodochrous DSM 43269 was investigated for a large range of different ketone substrates. These studies revealed that this enzyme not only oxygenates steroids, but also ketone moieties of a series of other open-chain ketones, such as cyclohexyl methyl ketone, cyclopentyl methyl ketone, and 3-acetylindole. Furthermore, the STMO catalyzed the oxygenation of cyclobutanone derivatives. Comparative biotransformations with recombinant Escherichia coli resting cells harboring the STMO, the cycloalkanone monooxygenase (CAMO) from Cylindrocarpon radicicola or the cyclohexanone monooxygenase (CHMO) from Acinetobacter calcoaceticus revealed that the STMO is enantiodivergent compared to the CHMO-type. Moreover, the STMO resulted in a higher enantiomeric excess of the product lactones compared to the known BVMOs of the same enantiopreference, such as cyclopentanone monooxygenases. 相似文献
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113.
Marcus Richter Sebastian Hahn Dr. Evgenia Dmitrieva Dr. Frank Rominger Dr. Alexey Popov Prof. Dr. Uwe H. F. Bunz Prof. Dr. Xinliang Feng Dr. Reinhard Berger 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(5):1345-1352
Polycyclic aromatic azomethine ylides (PAMYs) are powerful building blocks in the bottom-up synthesis of internally nitrogen-containing polycyclic aromatic hydrocarbons (N-PAHs) through 1,3-cycloaddition reactions. In this work, the cycloaddition reaction of PAMYs to asymmetric ortho-quinones is presented, which, in contrast to the addition to symmetric para-quinones, facilitates subsequent condensation reactions and allows the synthesis of three helical N-PAHs with ullazine-quinoxaline ( UQ - 1 – 3 ) backbones. UQ - 1 and UQ - 2 possess two helical centers; however, single-crystal X-ray analysis together with the computational modeling of UQ - 3 elucidate the formation of only the thermodynamically most stable geometry with four helical centers in a (P,P,M,M) configuration. For the series UQ - 1 – 3 , the number of redox steps is directly correlated with the number of ullazine or quinoxaline units incorporated into the targeted molecular backbones. A detailed investigation of the spectroscopic and magnetic properties of the radical cation and anion as well as the dication and dianion species by in situ EPR/UV/Vis-NIR spectroelectrochemistry is provided. The excellent optical and redox properties combined with helical geometries render them possibly applicable as chiral emitter or ambipolar charge transport material in organic electronics. 相似文献
114.
Uwe Gaitzsch Hansjörg KlaußStefan Roth Ludwig Schultz 《Journal of magnetism and magnetic materials》2012,324(4):430-433
A 5M Ni-Mn-Ga single crystal was investigated, supplied by Adaptamat Ltd, Finland. Especially low temperature magnetic actuation as well as cyclic tensile-compression tests revealed promising properties, which provide useful insights for training concepts in polycrystalline materials. Successive compressions lead to a significant reduction of the twinning stress by a factor of two. 相似文献
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116.
Oliver Brücher Uwe Bergsträßer Harald Kelm Jens Hartung Marco Greb Ingrid Svoboda Hartmut Fuess 《Tetrahedron》2012,68(34):6968-6980
A cascade, composed of (i) oxovanadium(V)-catalyzed oxidation of bromide by tert-butyl hydroperoxide and (ii) stereoselective 6-endo-bromocyclization, affords 3-bromo-2-aryl-2,6,6-trimethyltetrahydropyrans from styrene-type tertiary alkenols in synthetically useful yields. (E)-Alkenols add the bromo- and the alkoxy substituent anti-selectively across the double bond, indicating a bromonium ion-mechanism for the ring closure. 6-endo-control of the alkenol cyclization thereby arises from the polar effect of the aryl substituent. Two methyl substituents bound to the alkene terminus are not similarly able to favor 6-endo-cyclization, because strain arising from methyl group repulsion, as the bromonium-activated π-bond and the hydroxyl oxygen approach, directs bromocyclization of tertiary prenyl-type substrates toward tetrahydrofuran formation. A hexasubstituted bromotetrahydropyran prepared from the oxidation/bromocyclization cascade served as starting material for synthesis of racemic aplysiapyranoid A, in a sequence of free radical and polar functional group interconversion. 相似文献
117.
Bali Barume Uwe Naeher Désirée Ruppen Philip Schütte 《Current Opinion in Green and Sustainable Chemistry》2016
The growing public awareness of conflict minerals used in consumer electronics and various other devices (e.g. GPS in vehicles, medical equipment, airplane equipment and instruments, etc.) is accompanied by increasing regulatory obligations for companies affected by different laws and certification standards e.g. Dodd Frank Act section 1502, the ICGLR Regional Certification, the OECD Due Diligence Guidance or the planned EU Certification regulation.The so called conflicts minerals are natural mineral resources such as tin, tantalum, tungsten and Gold (3TG) that are critical resources for the electronic and automotive industries but also for other industries (aviation, medical equipment, etc.).Extraction of the 3TGs is widespread and includes primary industrial mining and artisanal mining as well as recycling. 相似文献
118.
Kamel Abbas Izabela Cydzik Riccardo Del Torchio Massimo Farina Efrat Forti Neil Gibson Uwe Holzwarth Federica Simonelli Wolfgang Kreyling 《Journal of nanoparticle research》2010,12(7):2435-2443
Industrially manufactured titanium dioxide nanoparticles have been successfully radiolabelled with 48V by irradiation with a cyclotron-generated proton beam. Centrifugation tests showed that the 48V radiolabels were stably bound within the nanoparticle structure in an aqueous medium, while X-ray diffraction indicated
that no major structural modifications to the nanoparticles resulted from the proton irradiation. In vitro tests of the uptake
of cold and radiolabelled nanoparticles using the human cell line Calu-3 showed no significant difference in the uptake between
both batches of nanoparticles. The uptake was quantified by Inductively Coupled Plasma Mass Spectrometry and high resolution
γ-ray spectrometry for cold and radiolabelled nanoparticles, respectively. These preliminary results indicate that alterations
to the nanoparticles’ properties introduced by proton bombardment can be controlled to a sufficient extent that their further
use as radiotracers for biological investigations can be envisaged and elaborated. 相似文献
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120.
Uwe J. Meierhenrich Prof. Dr. Jean‐Jacques Filippi Dr. Cornelia Meinert Pierre Vierling Dr. Jason P. Dworkin Dr. 《Angewandte Chemie (International ed. in English)》2010,49(22):3738-3750
Recent major discoveries in membrane biophysics hold the key to a modern understanding of the origin of life on Earth. Membrane bilayer vesicles have been shown to provide a multifaceted microenvironment in which protometabolic reactions could have developed. Cell‐membrane‐like aggregates of amphiphilic molecules capable of retaining encapsulated oligonucleotides have been successfully created in the laboratory. Sophisticated laboratory studies on the origin of life now show that elongation of the DNA primer takes place inside fatty acid vesicles when activated nucleotide nutrients are added to the external medium. These studies demonstrate that cell‐like vesicles can be sufficiently permeable to allow for the intake of charged molecules such as activated nucleotides, which can then take part in copying templates in the protocell interior. In this Review we summarize recent experiments in this area and describe a possible scenario for the origin of primitive cells, with an emphasis on the elongation of encapsulated nucleotides. 相似文献