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151.
Naoya Morohashi Kohei Ebata Tetsutaro Hattori 《Journal of inclusion phenomena and macrocyclic chemistry》2018,90(3-4):279-285
Upon stirring inclusion crystals of p-tert-butylthiacalix[4]arene (2) in solvents with heating, guest compounds were efficiently desorbed to yield guest-free crystals. More specifically, upon treatment with methanol, the exchange of guest compounds with methanol in the crystals, followed by the desorption of the methanol afforded metastable host crystals 2β, whereas, upon treatment with heptane, the dissolution of the inclusion crystals and simultaneous crystallization of compound 2 afforded stable host crystals 2α. Further, a host crystal of p-tert-butylcalix[4]arene (1) was recovered by the treatment of 2:1 (host/guest) inclusion crystals of compound 1 with supercritical carbon dioxide (scCO2), and through the combination of the guest exchange of 1:1 inclusion crystals of compound 1 with hexane and scCO2 treatment of the resulting 2:1 inclusion crystals 12·hexane. Although the recovered host crystal of compound 1 contained a small amount of CO2, it could be reused for the inclusion of organic compounds. 相似文献
152.
Dr. Kosuke Ono Shunsuke Shimo Dr. Kohei Takahashi Dr. Nobuhiro Yasuda Dr. Hidehiro Uekusa Prof. Nobuharu Iwasawa 《Angewandte Chemie (International ed. in English)》2018,57(12):3113-3117
Dynamic interconversion between large covalent organic cages was achieved simply by heating or acid/base treatment. A mixture of the boroxine cages 12‐mer and 15‐mer was cleanly converted into a pyridine adduct of the 9‐mer boroxine cage upon treatment with pyridine, and the geometry of N‐coordinated boron atoms changed from trigonal to tetrahedral. The reverse reaction was achieved by heating or acid treatment. In this process, the larger boroxine cages 12‐mer and 15‐mer were found to be entropically favored owing to the release of free pyridine molecules from 9‐mer ?6 Py. 相似文献
153.
Enantioselective Denitrogenative Annulation of 1H‐Tetrazoles with Styrenes Catalyzed by Rhodium
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Takayuki Nakamuro Kohei Hagiwara Dr. Tomoya Miura Prof. Dr. Masahiro Murakami 《Angewandte Chemie (International ed. in English)》2018,57(19):5497-5500
Sulfonylation of 1H‐tetrazoles with triflic anhydride in the presence of chiral rhodium(II) carboxylate dimers causes denitrogenation to generate α‐azo rhodium(II) carbenoid species as new types of donor/acceptor carbenoids, which then readily react with styrenes to afford 3,5‐diaryl‐2‐pyrazolines with a high degree of enantioselectivity. 相似文献
154.
Gold‐Catalyzed Regiospecific C−H Annulation of o‐Ethynylbiaryls with Anthranils: π‐Extension by Ring‐Expansion En Route to N‐Doped PAHs
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Zhongyi Zeng Hongming Jin Dr. Kohei Sekine Dr. Matthias Rudolph Frank Rominger Prof. Dr. A. Stephen K. Hashmi 《Angewandte Chemie (International ed. in English)》2018,57(23):6935-6939
We describe a novel, short, and flexible approach to diverse N‐doped polycyclic aromatic hydrocarbons (PAHs) through gold‐catalyzed π‐extension of anthranils with o‐ethynylbiaryls as reagents. This strategy uses easily accessible starting materials, is simple due to high step and atom economy, and shows good functional‐group compatibility as well as scale‐up potential. Mechanistically, the tandem reaction is proposed to involve a nucleophilic addition/ring opening/regiospecific C?H annulation/protodeauration sequence terminated by a Friedel–Crafts‐type cyclization. Photophysical studies of the products indicated violet‐blue fluorescence emission with quantum yields up to 0.45. 相似文献
155.
Cover Picture: Catalyst‐Enabled Site‐Divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl Acceptors (Angew. Chem. Int. Ed. 17/2018)
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156.
Utilization of Donor–Acceptor Interactions for the Catalytic Acceleration of Nucleophilic Additions to Aromatic Carbonyl Compounds
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Tatsuhiro Uchikura Dr. Kosuke Ono Dr. Kohei Takahashi Prof. Nobuharu Iwasawa 《Angewandte Chemie (International ed. in English)》2018,57(8):2130-2133
A conceptually new method for the catalytic electrophilic activation of aromatic carbonyl substrates, by utilizing donor–acceptor interactions between an electron‐deficient macrocyclic boronic ester host ( [2+2] BTH‐F ) and an aromatic carbonyl guest substrate, was realized. In the presence of a catalytic amount of [2+2] BTH‐F , dramatic acceleration of the nucleophilic addition of a ketene silyl acetal towards either electron‐rich aromatic aldehydes or ketones was achieved. Several control experiments confirmed that inclusion of the aromatic substrates within [2+2] BTH‐F , through efficient donor–acceptor interactions, is essential for the acceleration of the reaction. 相似文献
157.
The right-hand heterocyclic cores of oxazolomycins having either 16R or 16S-methyl group configurations on the β-lactones were stereoselectively synthesized from the common intermediate utilized for our previous syntheses of neooxazolomycin and oxazolomycin A. In addition, the right-hand segment required for the synthesis of KSM-2690 and lajollamycin members was also synthesized in a stereoselective manner. 相似文献
158.
Two-dimensional chirality at naturally chiral gold single crystalline surfaces was detected and characterized using optical second harmonic generation (SHG) measurements. SHG rotational anisotropy (SH-RA) patterns at Au(643)S and Au(643)R surfaces were mirror symmetric to each other. Systematic SH-RA measurements at chiral Au(hkl) surfaces with the same step and kink structures but different (111) terrace widths showed a linear correlation between surface step density and SH-RA fitting parameters arising from defects. These results indicate that SH-RA measurements provide information not only on surface chirality but also on density of surface defects. 相似文献
159.
[reaction: see text] A cyclic phosphoric acid derivative, derived from (R)-BINOL, was used as a chiral Br?nsted acid (10 mol %) in hydrophosphonylation of aldimines with diisopropyl phosphite at room temperature. Alpha-amino phosphonates were obtained with good to high enantioselectivities. 相似文献
160.
Kohei Sanui Tomohiko Asahara Naoya Ogata 《Journal of polymer science. Part A, Polymer chemistry》1968,6(5):1195-1207
Acrylates, such as ethyl acrylate, add with amino alcohol to form N-(hydroxyalkyl) β-alanine ester and room-temperature polycondensation follows, forming polyamide in the presence of a basic catalysts, such as alkali metal alkoxide. The reaction medium has an influence on the course of the polycondensation; that is, N-(hydroxyalkyl) polyamide is formed in methanol solution and polyamide ether in other solvents, such as tetrahydrofuran. These two courses of the room-temperature polycondensation have been studied, and the reaction mechanism is discussed in this paper. 相似文献