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81.
An enantioselective unified strategy for the syntheses of the oxylipin class of natural products was accomplished. Our strategy relies on three catalytic steps: (a) organocatalytic cyclopropanation, (b) the catalytic asymmetric transfer hydrogenation (CATHy) reaction, and (c) the Nozaki-Hiyama-Kishi reaction. 相似文献
82.
Skyler Speakman Sriram Somanchi Edward McFowland III Daniel B. Neill 《Journal of computational and graphical statistics》2016,25(2):382-404
We present the penalized fast subset scan (PFSS), a new and general framework for scalable and accurate pattern detection. PFSS enables exact and efficient identification of the most anomalous subsets of the data, as measured by a likelihood ratio scan statistic. However, PFSS also allows incorporation of prior information about each data element’s probability of inclusion, which was not previously possible within the subset scan framework. PFSS builds on two main results: first, we prove that a large class of likelihood ratio statistics satisfy a property that allows additional, element-specific penalty terms to be included while maintaining efficient computation. Second, we prove that the penalized statistic can be maximized exactly by evaluating only O(N) subsets. As a concrete example of the PFSS framework, we incorporate “soft” constraints on spatial proximity into the spatial event detection task, enabling more accurate detection of irregularly shaped spatial clusters of varying sparsity. To do so, we develop a distance-based penalty function that rewards spatial compactness and penalizes spatially dispersed clusters. This approach was evaluated on the task of detecting simulated anthrax bio-attacks, using real-world Emergency Department data from a major U.S. city. PFSS demonstrated increased detection power and spatial accuracy as compared to competing methods while maintaining efficient computation. 相似文献
83.
84.
Raghavendra NM Thampi P Gurubasavarajaswamy PM Sriram D 《Chemical & pharmaceutical bulletin》2007,55(11):1615-1619
Several substituted-quinazolin-3(4H)-ones 8-11ad were synthesized by condensation of 2-chloro-N-(4-oxo-substituted-quinazolin-3(4H)-yl)-acetamides with various substituted imidazoles through one pot reaction. Elemental analysis, IR, (1)H-NMR and mass spectral data confirmed the structure of the newly synthesized compounds. Synthesized quinazolin-4-one derivatives were investigated for their antitubercular, antibacterial and antifungal activities. Some of the tested compounds showed good antitubercular activity. None of the synthesized compounds showed significant antibacterial and antifungal activity. 相似文献
85.
Monte Carlo simulations show that copolymers with uniformly (or periodically) distributed sticky comonomers collapse "cooperatively," abruptly forming a compact intermediate comprising a monomer shell surrounding a core of the aggregated comonomers. In comparison, random copolymers collapse through a relatively less-compact intermediate comprising a comonomer core surrounded by a fluffy monomer shell that densifies over a wide temperature range. This difference between the collapse pathways for random and uniform copolymers persists to higher chain lengths, where uniform copolymers tend to form multiple comonomer cores. In this paper, we describe the formation of such an intermediate state, and the subsequent collapse, by recognizing that these arise from the expected balance between comonomer aggregation enthalpy and loop formation entropy dictated by the chain microstructure. 相似文献
86.
Suchetha Shetty Dr. Noorullah Baig Dr. Muhieddine Safa Dr. Ridha Gharbi Dr. Santhanagopalan Sriram Dr. Firas Rasoul Prof. Dr. Bassam Alameddine 《ChemistryOpen》2021,10(10):1067-1073
We report the synthesis, characterization, and photophysical properties of novel metal oxide nanoparticles (NPs) coated with specially designed fluorescein substituents which are capped with electron-withdrawing groups. The fluorescein-coated nanoparticles were synthesized in excellent yields, and their structures were confirmed using various advanced spectroscopic, instrumental, and surface analysis techniques, revealing the formation of the target functionalized nanoparticles (FNPs) which show superior chemical and thermal stabilities. In addition, the photophysical properties of the FNPs were examined using UV-visible absorption and fluorescence spectroscopy. These latter techniques disclosed aggregation-induced emission (AIE) properties for most of the target FNPs, namely those which are soluble in common organic solvents at selective concentration ranges of water fractions in the solvent mixture. 相似文献
87.
Dogamanti Ashok Chiranjeevi Pamula Aamate Vikas Kumar Vagolu Siva Krishna Sriram Dharmarajan Balasubramanian Sridhar Sarasija Madderla 《Molecular diversity》2021,25(4):2137-2148
Molecular Diversity - As part of an ongoing effort to develop new anti-tubercular agents, a series of novel indole-fused spirochromene hybrids (7a–l) were efficiently synthesized in excellent... 相似文献
88.
An efficient protocol has been developed for the synthesis of fused imidazo[2,1-a]isoindol-5-ones (2a–d) from 2-iodo benzoic acids and N,N-carbonyldiimidazole (CDI) using one-pot Pd-catalyzed C?C bond coupling. The reaction of imidazo[2,1-a]isoindol-5-one (2a–d) with substituted α-bromo ketones in toluene afforded corresponding imidazo[2,1-a]isoindolium derivatives (3a–i) in good yields. The structures of the title compounds were well established on the basis of infrared (IR), 1H NMR, carbon-13 nuclear magnetic resonance (13C NMR), mass spectral data, and elemental analysis (C, H, and N). In vitro antibacterial results revealed that, the compounds 3b and 3i were found to possess an excellent broad spectrum of inhibiting potency against all the tested bacterial strains with minimum inhibitory concentration values ranging from 3.125 to 25?µg mL?1. 相似文献
89.
The syntheses of enantiomer‐enriched orthogonally protected different (2S)‐2,3‐diaminopropanoates and unnatural furyl‐substituted (tert‐butoxy)carbonyl (Boc) as well as (benzyloxy)carbonyl (Cbz) protected amino acid esters are accomplished by means of an enantioselective aza‐Henry reaction. A key feature of this protocol is organocatalysis as a genesis of chirality to ensure high enantioselectivity. 相似文献
90.
A simple and practical procedure for the synthesis of aza- and oxacycles, which possess an array of stereogenic functionalities, is described. This protocol relies on tandem Cu-catalyzed coupling of suitably functionalized terminal alkyne with diazoester followed by isomerization and subsequent aza or oxa-Michael reaction, thus generating the required scaffold with high diastereoselectivity. 相似文献