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151.
Takeshi Takeda Shuichi Kuroi Makoto Ozaki Akira Tsubouchi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5-6):1291-1296
Abstract Trialkylsilyl group-directed regioselective transformations of alkynyl thioacetals to alkynylcyclopropanes and enynes are described. 相似文献
152.
Asei William Kawaguchi Atsushi Sudo Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2014,52(3):410-416
1,3‐benzoxazine 1 , bearing 4‐pyridyl moiety on the nitrogen atom, was synthesized from p‐cresol, 4‐aminopyridine, and paraformaldehyde. The efficient synthesis was achieved by adding acetic acid to suppress the strong basicity caused by the presence of 4‐aminopyridine derivatives. Upon heating 1 at 180 °C, it underwent the thermally induced ring‐opening polymerization. The resulting polymer was composed of two types of repeating unit, i.e., (1) Mannich‐type one (‐phenol‐CH2‐NR‐CH2‐) that can be expected from the general ring‐opening polymerization of conventional benzoxazines and (2) a typical phenolic resin‐type one (‐phenol‐CH2‐phenol‐) induced by release of 4‐aminopyridine and paraformaldehyde (unit B). Another structural feature of the polymer was that it possessed a benzoxazine moiety at the chain end. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 410–416 相似文献
153.
Total Synthesis of the 7,10‐Epimer of the Proposed Structure of Amphidinolide N,Part II: Synthesis of C17–C29 Subunit and Completion of the Synthesis 下载免费PDF全文
Dr. Koji Ochiai Dr. Sankar Kuppusamy Yusuke Yasui Kenji Harada Dr. Nishant R. Gupta Dr. Yohei Takahashi Prof. Dr. Takaaki Kubota Prof. Dr. Jun'ichi Kobayashi Prof. Dr. Yujiro Hayashi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(10):3287-3291
The total synthesis of 7,10‐epimer of the proposed structure of amphidinolide N was accomplished. The requisite chiral C17–C29 subunit was assembled stereoselectively via Keck allylation, Shi epoxidation, diastereoselective 1,3‐reduction, and a later oxidative synthesis of the THF framework. The C1–C13 and C17–C29 subunits were successfully coupled using a Enders RAMP “linchpin” as the C14–C16 three carbon unit, thereby controlling the chirality at C14 and C16. The labile allyl epoxy moiety was successfully constructed by Grieco–Nishizawa olefination at a final stage of the synthesis. 相似文献
154.
Takeshi Eitoku Kazuya Taniguchi Yuta Nakazato Shunichi Ono Kenji Katayama 《Optical Review》2010,17(1):5-9
Formation process of gold nanoparticles was investigated by near-field heterodyne transient grating method. In the absence
of the protective agents, although the diffusion of H[AuICl2] could be observed after the photo-reduction of H[AuIIICl4], the diffusion of nanoparticle-seeds was not observed. On the other hand, in the presence of the protective agents, the
diffusion of a complex molecule (Au and protective agent) and nanoparticle-seeds could be observed. From these results, it
was found that enough amount of the complex is essential for the nanoparticle formation. We also investigated the formation
process with four different chemicals as a protective agent. The hydrodynamic radius of nanoparticle-seeds generated in the
poly(vinyl pyrrolidone) and TritonX-100 solutions were larger than those generated in the Tween 20 and Brij 58 solutions.
The former two have hydrophilic chain in the molecular structure; on the other hand, the latter two have hydrophobic alkyl
chain. Based on those facts, we concluded that the interaction between the chains of the complex molecule plays an important
role in the nanoparticle formation process. 相似文献
155.
156.
Fujiko Iwasaki Seui Kakuma Satoshi Yoshida Shin Murata Masanori Yasui 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4):515-516
Abstract The deformation electron-density distributions of 6a-thia-1,3,4,6-tetraazapentalene derivatives (I, II) and bis(phenylthio)dibenzothiophene (III) were investigated by the X-ray diffraction method. For I and II, a structure around the hypervalent S-N bonds is a trigonal bipyramid with equatorial sp2 hybrid of S-C bond and lone-pair electrons and apical polarized S-N bonds. In 111 lone-pair electron densities are observed perpendicular to the thiophene ring and the C-S-C sulfide planes. 相似文献
157.
Makoto Okawara Takeshi Endo Eisuke Fujiwara Takayoshi Hirose 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(4):441-459
Polymers containing 1,4-dihydronicotinamide (P-NAH) alloxan (P-A), and viologen (P-V2+) moieties were synthesized and characterized. P-NAH reduced various organic substances such as lipoic acid, alloxan, and viologens and also immobilized quinone mediated by alloxan. P-A was reduced to the polymer-bearing alloxan radical and the dialuric acid structure without crosslinks by one- and two-electron reduction, respectively, and P-A also mediated the redox reaction occurring between aqueous and organic (water-immiscible) layers. P-V2+ was converted to the stable viologen radical reversibly by one-electron reduction. Electric potentials and currents on photo-reduction of P-V2+ and catalytic behavior of P-V2+ in the reduction of carbonyl compounds were examined. 相似文献
158.
Hiroyuki Nishide Naoki Yoshioka Yukoh Saitoh Ritsuko Gotoh Takeshi Miyakawa Eishun Tsuchida 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(9):775-786
Abstract m- and p Bis(diphenylene)propenylphenylacetylene (m-, p-8) were synthesized and polymerized with WCI6, MoCl5, and Rh catalyst, yielding solvent-soluble poly(phenylacetylene)s bearing a π-conjugated bis(di-phenylene)propenyl groups (m-, p-7a). The polymers gave their polyanion derivatives, which were electrolytically and chemically oxidized to yield the corresponding polyradicals (m-, p-7b). The polyradicals were chemically very stable due to the resonance stabilization of an unpaired electron whose spin concentration could be increased up to ca. 2 × 1023 spins per molar monomer unit. ESR spectroscopy suggested an antiferro-magnetic interaction between unpaired electrons. 相似文献
159.
160.
Experimental detection of proteolytic activity in a signal peptide peptidase of Arabidopsis thaliana
Hoshi Masako Ohki Yu Ito Keisuke Tomita Taisuke Iwatsubo Takeshi Ishimaru Yoshiro Abe Keiko Asakura Tomiko 《BMC biochemistry》2013,14(1):1-8