排序方式: 共有48条查询结果,搜索用时 31 毫秒
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Dr. Ryu Yamasaki Dr. Masato Ohashi Kyotaro Maeda Takuya Kitamura Minami Nakagawa Korehito Kato Tetsushi Fujita Ryohei Kamura Kazuto Kinoshita Dr. Hyuma Masu Prof. Dr. Isao Azumaya Prof. Dr. Sensuke Ogoshi Prof. Dr. Shinichi Saito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(10):3415-3425
A detailed study of the Ni‐catalyzed [4+3+2] cycloaddition reaction between ethyl cyclopropylideneacetate and dienynes has been conducted, resulting in the development of a new method for the synthesis of compounds containing nine‐membered rings. We studied the reactivity of various dienynes, together with their substituent and conformational effects. The mechanism of the reaction was probed by examining the stoichiometric reactions of the Ni complexes and dienynes. 相似文献
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Chiral Bis(imidazolidine)‐Derived NCN Pincer Rh Complex for Catalytic Asymmetric Mannich Reaction of Malononitrile with N‐Boc Imines
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Prof. Dr. Takayoshi Arai Takuma Moribatake Prof. Dr. Hyuma Masu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(30):10671-10675
Chiral bis(imidazolidine)‐derived NCN–rhodium complexes ([PhBidine‐RhX2] and [tBu‐PhBidine‐RhX2]) were prepared by a C?H insertion method, and the structures were unequivocally determined by X‐ray crystallographic analysis. The [tBu‐PhBidine‐Rh(OAc)2] complex smoothly catalyzed an asymmetric Mannich reaction of malononitrile with N‐Boc imines to give products in up to 94 % ee, which are useful for the synthesis of chiral α‐amino acids. 相似文献
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Iwao Okamoto Masayuki TerashimaHyuma Masu Mayumi NabetaKaori Ono Nobuyoshi MoritaKosuke Katagiri Isao AzumayaOsamu Tamura 《Tetrahedron》2011,67(44):8536-8543
A series of cis-preferential aromatic N-methyl amides was designed and synthesized, and acid-induced conformational alteration of these compounds was investigated by means of NMR measurements in solution and X-ray crystal structure analysis. Compounds with a terminal N-methyl-N-(2-pyridyl) amide unit showed acid-induced conformational change from cis to trans, while those with a terminal N-methyl-2-pyridinecarboxamide unit showed a change of the carbonyl orientation from anti to syn with retention of cis conformation. 相似文献
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[reaction: see text]. Cycloaddition of aziridines with isocyanates proceeded smoothly in the presence of a nickel catalyst, and five iminooxazolidine derivatives were isolated in good yields. The best result was obtained when the reaction was carried out in the presence of NiI2, and a longer reaction time allowed the isomerization of the iminooxazolidine to the corresponding imidazolidinone derivatives. 相似文献
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Frustrated Helicity: Joining the Diverging Ends of a Stable Aromatic Amide Helix to Form a Fluxional Macrocycle
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Ko Urushibara Dr. Yann Ferrand Dr. Zhiwei Liu Prof. Hyuma Masu Prof. Vojislava Pophristic Prof. Aya Tanatani Prof. Ivan Huc 《Angewandte Chemie (International ed. in English)》2018,57(26):7888-7892
Macrocyclization of a stable two‐turn helical aromatic pentamide, that is, an object with diverging ends that are not prone to cyclization, was made possible by the transient introduction of disruptors of helicity in the form of acid‐labile dimethoxybenzyl tertiary amide substituents. After removal of the helicity disruptors, NMR, X‐ray crystallography, and computational studies show that the macrocycle possesses a strained structure that tries to gain as high a helical content as possible despite being cyclic. Two points of disruption of helicity remain, in particular a cis amide bond. This point of disruption of helicity can propagate along the cycle in a fluxional manner according to defined trajectories to produce ten degenerate conformations. 相似文献
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Nuclear magnetic resonance studies of alkaline earth phosphosilicate and aluminoborosilicate glasses
Hiroshi Yamashita Hidetake Yoshino Keishi Nagata Hyuma Inoue Takeshi Nakajin Takashi Maekawa 《Journal of Non》2000,270(1-3):48-59
The 11B, 27Al, 29Si and 31P magic angle spinning (MAS) NMR spectra of MO–P2O5, MO–SiO2–P2O5 and MO(M′2O)–SiO2–Al2O3–B2O3 (M=Mg, Ca, Sr and Ba, M′=Na) glasses were examined. In binary MO–P2O5 (M=Ca and Mg) glasses, the distributions of the phosphate sites, P(Qn), can be expressed by a theoretical prediction that P2O5 reacts quantitatively with MO. In the ternary 0.30MO–0.05SiO2–0.65P2O5 glasses, the 6-coordinated silicon sites were detected, whose population increases in the order of MgOxCaO–0.05SiO2–(0.95−x)P2O5 glasses, its population increases with an increase in f (=([P2O5]−[MO]−[B2O3]−[Na2O])/[SiO2]) and has maximum at f=9. The signal due to the 5-coordinated silicon atoms is also observed when x is smaller than 0.45. When three network-forming oxides such as SiO2, Al2O3 and B2O3 coexist, Al2O3 reacts preferably with MO. The populations of 4-coordinated boron atoms, N4, are expressed well with r/(1−r), where r=([Na2O]−[Al2O3])/([Na2O]−[Al2O3]+[B2O3]). The correlation of the Raman signal at 1210 and 1350 cm−1 with the NMR signal of Si(Q6) at −215 ppm is also seen. 相似文献
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Mayumi B. Takeyama Atsushi Noya Shozo Kambara Yuichiro Hayasaka Hideaki Machida Kazuya Masu 《Applied Surface Science》2009,256(4):1222-1226
We have prepared thin Zr-B films at low temperatures as a new material applicable to an extremely thin barrier against Cu diffusion in Si-ULSI metallization. The obtained Zr-B films mainly consist of the ZrB2 phase with a nanocrystalline texture on SiO2 and a fiber texture on Cu. The resistivity of the Zr-B films depends on the substrate of SiO2 or Cu. The constituent ratio of B/Zr is almost 2, though the contaminants of oxygen, nitrogen, and carbon are incorporated in the film. The nanocrystalline structure of the Zr-B film on SiO2 is stable due to annealing at temperatures up to 500 °C for 30 min. We applied the 3-nm thick Zr-B film to a diffusion barrier between Cu and SiO2, and the stable barrier properties were confirmed. We can demonstrate that the thin Zr-B film is a promising candidate for thin film application to a metallization material in Si-ULSIs. 相似文献
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Synthetic studies of two components of tubulysins, tubulin polymerization inhibitors are described. The highly stereoselective synthesis of tubuvaline methyl ester (2) was accomplished by 1,3-dipolar cycloaddition of nitrone d-6 and acrylic acid derivatives 7 as a key step. The synthesis of tubuphenylalanine (3) was conducted by an aldol reaction of a boron enolate of (S)-4-isopropyl-3-propionyl-2-oxazolidinone (13) with aldehyde 14, readily prepared from phenylalanine, followed by Barton deoxygenation under radical conditions. 相似文献
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The Ni-catalyzed [3+2+2] cocyclization between ethyl cyclopropylideneacetate (1) and 1,3-diynes afforded cycloheptadiene derivatives. The three-component reaction of 1, 1,3-diynes, and alkynes proceeded with good yield and high selectivity. Scope of the substrates was studied, and the origin of chemo- and regioselectivity of the reaction is discussed. 相似文献