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21.
Expedient and Diastereodivergent Assembly of Terpenoid Decalin Subunits having Quaternary Stereocenters through Organocatalytic Robinson Annulation of Nazarov Reagent
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Barbara Berkes Kristóf Ozsváth Laura Molnár Tamás Gáti Tamás Holczbauer György Kardos Tibor Soós 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(50):18101-18106
We report an expedient approach to highly functionalized cis‐ and trans‐decalines that could function as key structural subunits toward the synthesis of various classes of terpenoids. Key to the strategy is an organocatalyzed Robinson annulation reaction of the Nazarov reagent that affords chiral enone building blocks with high enantioselectivities. The quaternary carbon stereogenic center can direct the subsequent reactions and allow the rapid and diastereoconvergent assembly of complex decalines with contiguous stereocenters. 相似文献
22.
A. S. Barabash V. Ya. Bradnova V. V. Dubinina N. P. Egorenkova S. I. Konovalov E. A. Pozharova N. G. Polukhina V. A. Smirnitskii N. I. Starkov Tan Nang So M. M. Chernyavskii T. V. Shchedrina V. I. Yumatov 《Bulletin of the Lebedev Physics Institute》2012,39(10):300-304
Ranges of monochromatic muons in nuclear photoemulsion, produced in the ?? ?? ??? ?? decay, are measured by the coordinate method to determine their energy by the range. The variance of the muon energymeasured by this method ?? ?? = (0.11±0.01) MeV, which corresponds to the accuracy of the determination of the charged particle energy by the range in nuclear emulsion ??3.1%. The developed technique will allow electron energy measurements in the 2??-decay (??3 MeV)with an accuracy of (5?C6)%. 相似文献
23.
Chang-Ho Kang Sang-Hyun Han YuJin Shin Soo Ji Oh Jae-Seong So 《Applied biochemistry and biotechnology》2014,172(6):2907-2915
Contamination by Cd is a significant environmental problem. Therefore, we examined Cd removal from an environmental perspective. Ureolysis-driven calcium carbonate precipitation has been proposed for use in geotechnical engineering for soil remediation applications. In this study, 55 calcite-forming bacterial strains were newly isolated from various environments. Biomineralization of Cd by calcite-forming bacteria was investigated in laboratory-scale experiments. A simple method was developed to determine the effectiveness of microbially induced calcite precipitation (MICP). Using this method, we determined the effectiveness of biomineralization for retarding the flow of crystal violet through a 25-mL column. When the selected bacteria were analyzed using an inductively coupled plasma optical emission spectrometer, high removal rates (99.95 %) of Cd were observed following incubation for 48 h. Samples of solids that formed in the reaction vessels were examined using a scanning electron microscope. The CdCO3 compounds primarily showed a spherical shape. The results of this study demonstrate that MICP-based sequestration of soluble heavy metals via coprecipitation with calcite may be useful for toxic heavy metal bioremediation. 相似文献
24.
Majchrzak-Kucęba Izabela Sołtysik Marcelina 《Journal of Thermal Analysis and Calorimetry》2020,141(1):267-275
Journal of Thermal Analysis and Calorimetry - The pressure drop is one of the most important factors leading to the distribution of refrigerant in the micro-channel heat exchanger. The main... 相似文献
25.
Order - A modular semilattice is a semilattice generalization of a modular lattice. We establish a Birkhoff-type representation theorem for modular semilattices, which says that every modular... 相似文献
26.
Thermal stability of ester linkage in the presence of 1,2,3‐Triazole moiety generated by click reaction
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Kyu Seong Lee So Yeong Park Hong Chul Moon Jin Kon Kim 《Journal of polymer science. Part A, Polymer chemistry》2017,55(3):427-436
The copper(I)‐catalyzed alkyne‐azide cycloaddition (CuAAC), so‐called “click” reaction, is one of most useful synthetic strategies to connect two polymer chains. 1,2,3‐Triazole ring (TA) produced by the click reaction has good thermal and chemical stability. However, we observed that block copolymers synthesized by the click reaction showed thermal degradation to give homopolymers when they are thermally annealed at high temperature, which is required for obtaining equilibrium microdomain structure. To investigate the origin of thermal instability of block copolymers, we synthesized model polystyrenes (PSs) using systematically designed bi‐functional atom transfer radical polymerization (ATRP) initiators containing TA. PS including both ester and TA groups showed thermal decomposition at relatively low temperature (e.g., 140 °C). MALDI‐TOF analysis clearly demonstrated that the cleavage site is the ester group adjacent to TA. We also found that the bromine group located at the polymer chain end plays an important role in pyrolysis of ester groups at low temperature. The pyrolysis occurs by syn‐elimination of the ester group. This result implies that the phase behavior of block copolymer synthesized by click reaction should be carefully investigated when high temperature thermal annealing is required. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 427–436 相似文献
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Hui‐Xian Yeong Dr. Hong‐Wei Xi Dr. Yongxin Li Prof. Dr. Kok Hwa Lim Dr. Cheuk‐Wai So 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(35):11786-11790
The synthesis and reactivity of a silyliumylidene cation stabilized by an amidinate ligand and 4‐dimethylaminopyridine (DMAP) are described. The reaction of the amidinate silicon(I) dimer [ L Si:]2 ( 1 ; L =PhC(NtBu)2) with one equivalent of N‐trimethylsilyl‐4‐dimethylaminopyridinium triflate [4‐NMe2C5H4NSiMe3]OTf and two equivalents of DMAP in THF afforded [ L Si(DMAP)]OTf ( 2 ). The ambiphilic character of 2 is demonstrated from its reactivity. Treatment of 2 with 1 in THF afforded the disilylenylsilylium triflate [ L′ 2( L )Si]OTf ( 3 ; L′ = L Si:) with the displacement of DMAP. The reaction of 2 with [K{HB(iBu)3}] and elemental sulfur in THF afforded the silylsilylene [ L SiSi(H){(NtBu)2C(H)Ph}] ( 4 ) and the base‐stabilized silanethionium triflate [ L Si(S)DMAP]OTf ( 5 ), respectively. Compounds 2 , 3 , and 5 have been characterized by X‐ray crystallography. 相似文献
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