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991.
Dr. Yoshinori Tokairin Yuhei Shigeno Dr. Jianlin Han Prof. Dr. Gerd-Volker Röschenthaler Dr. Hiroyuki Konno Dr. Hiroki Moriwaki Vadim A. Soloshonok 《ChemistryOpen》2020,9(1):93-96
Four differently substituted chiral Ni(II)-complexes of dehydroalanine Schiff base were prepared and reacted with BrCF2COOEt/Cu under the standard reaction conditions. The observed diastereoselectivity was found to depend on the degree and pattern of chlorine substitution for hydrogen in the structure of the dehydroalanine complexes. The unsubstituted complex gave the ratio of diastereomers (S)(2S)/(S)(2R) of 66/34. On the other hand, introduction of chlorine atoms in the strategic positions on the chiral ligands allowed to achieve a practically attractive diastereoselectivity of (∼98.5/1.5). Diastereomerically pure major product was disassembled to prepare 9-fluorenylmethyloxycarbonyl (Fmoc) derivative of (S)-4,4-difluoroglutamic acid. 相似文献
992.
Dr. Yuma Otake Yusuke Shibata Dr. Yoshihiro Hayashi Prof. Dr. Susumu Kawauchi Prof. Dr. Hiroyuki Nakamura Prof. Dr. Shinichiro Fuse 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(31):13025-13030
The development of a robust amide-bond formation remains a critical aspect of N-methylated peptide synthesis. In this study, we synthesized a variety of dipeptides in high yields, without severe racemization, from equivalent amounts of amino acids. Highly reactive N-methylimidazolium cation species were generated in situ to accelerate the amidation. The key to success was the addition of a strong Brønsted acid. The developed amidation enabled the synthesis of a bulky peptide with a higher yield in a shorter amount of time compared with the results of conventional amidation. In addition, the amidation can be performed by using either a microflow reactor or a conventional flask. The first total synthesis of naturally occurring bulky N-methylated peptides, pterulamides I–IV, was achieved. Based on experimental results and theoretical calculations, we speculated that a Brønsted acid would accelerate the rate-limiting generation of acyl imidazolium cations from mixed carbonic anhydrides. 相似文献
993.
994.
Chihiro Suzuki Izumi Murakami Fumihiro Koike Takeshi Higashiguchi Hiroyuki A. Sakaue Naoki Tamura Shigeru Sudo Gerry O'Sullivan 《X射线光谱测定》2020,49(1):78-84
We are developing an experimental database of extreme ultraviolet spectra from highly charged ions using optically thin high-temperature plasmas produced in the Large Helical Device. Spectra from a variety of elements with atomic numbers ranging from 36 to 83 have been systematically recorded in the range of 1–20 nm by a grazing incidence spectrometer. For higher Z elements from tin onward, discrete or quasicontinuum spectral features from n=4 (N-shell) ions are mainly observed depending upon the plasma temperature, which leads to some new experimental identifications of spectral lines. On the other hand, major emitters are n=3 (M-shell) ions for medium Z elements from krypton to ruthenium. The calculated wavelengths for Δn≠0 transitions agree well with the measurements and the calculated wavelengths are systematically shifted to shorter wavelengths for Δn=0 transitions associated with inner-subshell excited configurations. 相似文献
995.
Prof. Hidemitsu Uno Kota Muramatsu Shogo Hiraoka Hiroyuki Tahara Mako Hirose Eidai Tamura Tatsumi Shiraishi Dr. John Mack Prof. Nagao Kobayashi Dr. Shigeki Mori Dr. Tetsuo Okujima Dr. Masayoshi Takase 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(25):5701-5708
A bicyclo[2.2.2]octadiene(BCOD)-fused bis(dipyrromethane) derivative was reacted with methylal in the presence of trifluoroacetic acid followed by oxidation with chloranil to give a doubly N-confused phlorin derivative, which did not undergo the retro-Diels–Alder reaction extruding an ethylene molecule on heating. In contrast, a 7-tert-butoxybicyclo[2.2.1]heptadiene(7-BuOBCHD)-fused bis(dipyrromethane) yielded benzene-ring-fused doubly N-confused porphyrins by following similar reaction sequences. 相似文献
996.
Jun Zhang Dr. Wataru Kosaka Prof. Dr. Susumu Kitagawa Prof. Dr. Masaki Takata Prof. Dr. Hitoshi Miyasaka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(12):3020-3031
Optimal control of gas adsorption properties in metal–organic frameworks (MOFs) or porous coordination polymers (PCPs) remains a great challenge in the field of materials science. An efficient strategy to capture electron-acceptor-type gas molecules such as nitrogen monooxide (NO) is to use host–guest interactions by utilizing electron-donor-type MOFs/PCPs as host frameworks. Herein, we focus on a highly electron-donating chain compound by using the paddlewheel-type [Ru2II,II] complex [Ru2(2,4,5-Me3PhCO2)4] (2,4,5-Me3PhCO2−=2,4,5-trimethylbenzoate) with the phenazine (phz) linker: [Ru2(2,4,5-Me3PhCO2)4(phz)] ( 1 ). Compound 1 exhibited a specific gated adsorption for NO under gas pressures greater than 60 kPa at 121 K, which finally resulted in approximately seven molar equivalents being taken up at 100 kPa followed by four molar equivalents remaining under vacuum at 121 K; its Rh isomorph ( 2 ) with weaker donation ability was inactive for NO. When the sample of 1 ⊃4 NO was heated to room temperature, the compound underwent a crystal-to-crystal phase transition to give [Ru2(2,4,5-Me3PhCO2)4(NO)2](phz) ( 1 -NO), involving a post-synthetic nitrosylation on the [Ru2] unit, accompanied by an eventful site-exchange with phz. This drastic event, which is dependent on the NO pressure, temperature, and time, was coherently monitored by using several different in situ techniques, revealing that the stabilization of NO molecules in nanosized pores dynamically and stepwisely occurred with the support of strong electronic/magnetic host–guest interactions. 相似文献
997.
Takuma Tahara Dr. Shuichi Suzuki Prof. Dr. Masatoshi Kozaki Prof. Dr. Daisuke Shiomi Dr. Kenji Sugisaki Prof. Dr. Kazunobu Sato Prof. Dr. Takeji Takui Yota Miyake Prof. Dr. Yuko Hosokoshi Prof. Dr. Hiroyuki Nojiri Prof. Dr. Keiji Okada 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(29):7201-7209
The spin–spin and magnetic properties of two (nitronyl nitroxide)-(di-p-anisylamine-phenothiazine) diradical cation salts, ( DAA-PTZ ) + -NN⋅ MBr4− (M=Ga, Fe), have been investigated. These diradical-cation species were prepared by the cross-coupling of iodophenothiazine DAA-PTZ-I with NN-AuPPh3 followed by oxidation with the thianthrenium radical cation ( TA+⋅ MBr4−). These salts were found to be highly stable under aerobic conditions. For the GaBr4 salt, large ferromagnetic intramolecular and small antiferromagnetic intermolecular interactions (J1/kB=+320 K and J2/kB=−2 K, respectively) were observed. The magnetic property of the Fe3+ salt was analyzed by using a six-spin model assuming identical intramolecular exchange interaction (J3/kB=+320 K) and the other exchange interactions (J4/kB=−7 K and J5/kB=−4 K). A significant color change was observed in the UV/Vis/NIR absorption spectra upon electrochemical oxidation of the doublet DAA-PTZ-NN to the triplet ( DAA-PTZ ) + -NN . 相似文献
998.
Yasuhiro Tsukada Hiroyuki Furutani Yoshikazu Abe Keishi Monda Motoi Kawatsura 《Tetrahedron letters》2006,47(11):1801-1804
Various types of differently fluorinated-alkyl sulfate ionic liquids have been prepared; the hydrophobicity was dependent on the content ratio of the fluorine on the alkyl sulfate anion and 2,2,3,3,4,4,5,5-octafluoropentyl sulfate salts showed hydrophobic properties. Melting point and viscosity were also dependent on the fluorine contents of the anionic part, while conductivity was determined by the cationic part and not influenced by the fluorine contents. Efficient lipase-catalyzed transesterification was demonstrated using hydrophobic 1-butyl-3-methylimidazolim 2,2,3,3,4,4,5,5-octafluoropentyl sulfate ([bmim][C5F8]) as solvent. 相似文献
999.
Motomasa Kobayashi Nobuyoshi Shimizu Isao Kitagawa Yoshimasa Kyogoku Nobuyuki Harada Hisashi Uda 《Tetrahedron letters》1985,26(32):3833-3836
The absolute stereostructures of two pentacyclic hydroquinones, halenaguinol () and halenaquinol sulfate () from the Okinawan marine sponge Xestospongia sapra, have been determined by means of theoretical calculation of CD spectra. 相似文献
1000.
Thermoanalytical investigations on the two component system of L-dipalmitoyl phosphatidylcholine and water revealed that the sub-transition in the present system is remarkably affected by the water content as well as the condition of annealing treatment and also that the stable low-temparature phase obtained after the appropriate annealing shows the existence of the more loosely-bound water than that in the super-cooled Lβ′ phase. 相似文献