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1.
Zev Lidert 《Tetrahedron》1981,37(5):967-969
Raman and 1H NMR spectroscopic data obtained for a dimeric product 4c formed on iodine oxidation of N-pnenyl-N-thiomethyl-thioglycolic acid amide (3c) indicate that this product is 4,11-diphenyl-4,11-diaza-1,2,7,8-tetrathia-cyclododecane-5,10-dione. The barrier to interconversion between the conformers of 4c has been determined by DNMR. The height of the barrier (ΔG≠ = 17.3 ±0.1 ) is in agreement with the proposed structure. This investigation thus gives a support to the previously proposed mechanism of regiospecific dimeric oxidations of unsymmetrical dithols of type 3c. 相似文献
2.
Shane M. Hickey Shani K. Tripcony Rui Li Richard J. Williams 《Supramolecular chemistry》2015,27(5-6):425-435
Using the rigid norbornane scaffold, a series of low-molecular-weight organogelators has been synthesised and evaluated. Three separate compounds (16, 19 and 20) were identified as organogelators in three aromatic organic solvents (PhMe, anisole and o-xylene). The formation of fibrillar assemblies at nanometre level was confirmed using atomic force microscopy and transmission electron microscopy. 相似文献
3.
The chemical behavior and some physical properties (dipole moment, IR. vs. Raman spectra) of the titled compound are not fully consistent with a strictly centrosymmetric structure which might be expected for the anti configuration. The carbonyl groups are less reactive toward nucleophilic reagents and sp2 → sp3 transformations as compared to cyclopentanone systems. 相似文献
4.
Shani Smith Charles GiesekerRenate Reimschuessel Christie-Sue DeckerMary C. Carson 《Journal of chromatography. A》2009,1216(46):8224-8232
LC-ion trap mass spectrometry was used to screen and confirm 38 compounds from a variety of drug classes in four species of fish: trout, salmon, catfish, and tilapia. Samples were extracted with acetonitrile and hexane. The acetonitrile phase was evaporated, redissolved in water and acetonitrile, and analyzed by gradient chromatography on a phenyl column. MS2 or MS3 spectra were monitored for each compound. Qualitative method performance was evaluated by the analysis over several days of replicate samples of control fish, fish fortified with a drug mixture at 1 ppm, 0.1 ppm and 0.01 ppm, and fish dosed with a representative from each drug class. Half of the 38 drugs were confirmed at 0.01 ppm, the lowest fortification level. This included all of the quinolones and fluoroquinolones, the macrolides, malachite green, and most of the imidazoles. Florfenicol amine, metronidazole, sulfonamides, tetracyclines, and most of the betalactams were confirmed at 0.1 ppm. Ivermectin and penicillin G were only detectable in the 1 ppm fortified samples. With the exception of amoxicillin, emamectin, metronidazole, and tylosin, residue presence was confirmed in all the dosed fish. 相似文献
5.
6.
Shani Sperinck Thomas Becker Kate Wright William R. Richmond 《Journal of inclusion phenomena and macrocyclic chemistry》2009,65(1-2):89-95
A solvothermal method has been used to prepare hybrid inorganic–organic composites with a lamellar structure in which layers of wurtzite ZnS are separated by intercalated diamine molecules. A hybrid composite prepared with diethylenetriamine has been isolated and characterised and its structure and properties compared with those of the composite prepared using ethylenediamine. Comparative structural and morphological studies of the two lamellar hybrid composites are described on the basis of powder XRD, electron and scanning probe microscopies and thermal analysis of the materials. 相似文献
7.
Selden NS Todhunter ME Jee NY Liu JS Broaders KE Gartner ZJ 《Journal of the American Chemical Society》2012,134(2):765-768
Cell adhesion organizes the structures of tissues and mediates their mechanical, chemical, and electrical integration with their surroundings. Here, we describe a strategy for chemically controlling cell adhesion using membrane-anchored single-stranded DNA oligonucleotides. The reagents are pure chemical species prepared from phosphoramidites synthesized in a single chemical step from commercially available starting materials. The approach enables rapid, efficient, and tunable cell adhesion, independent of proteins or glycans, by facilitating interactions with complementary labeled surfaces or other cells. We demonstrate the utility of this approach by imaging drug-induced changes in the membrane dynamics of non-adherent human cells that are chemically immobilized on a passivated glass surface. 相似文献
8.
Zev Lidert 《Tetrahedron letters》1985,26(30):3601-3604
A “push-pull” stabilized 3a-methyl-3aH-indene 1 and the first 3aH-indenoquinone 7 have been synthesized and characterized. 相似文献
9.
The translation of DNA sequences into synthetic products is a key requirement of our approach to evolving synthetic molecules through iterated cycles of translation, selection, and amplification. Here we report general linker and purification strategies for sequence-specific DNA-templated synthesis that collectively enable the product of a DNA-templated reaction to be isolated and to undergo subsequent DNA-templated reactions. Using these strategies, we have achieved the first multistep nucleic acid-templated small-molecule syntheses to generate two different molecules. In addition to representing a method for translating DNA templates sequence-specifically into corresponding multistep synthetic products, our findings also provide experimental support for previously proposed models invoking multistep nucleic acid-templated synthesis as mediating the prebiotic translation of replicable information into the earliest functional molecules. 相似文献
10.
The translation of DNA into synthetic molecules enables their manipulation by powerful evolution-based methods previously available only to proteins and nucleic acids. The development of increasingly sophisticated DNA-templated small-molecule syntheses is crucial to broadening the scope of this approach. Here, we report the translation of DNA templates into monocyclic and bicyclic N-acyloxazolidines using multistep DNA-templated organic synthesis. Second-generation template architectures, used for the first time in a multistep DNA-templated synthesis, together with reactions and linker cleavage strategies not previously described in a DNA-templated format, were crucial to the successful translation. The products generated in this work represent the most complex small molecules to date synthesized in a DNA sequence-programmed manner and provide the basis for DNA-templated synthetic heterocycle libraries. 相似文献