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121.
Akira Hirota Masahira Nakagawa Heiichi Sakai Akira Isogai Kazuo Furihata Haruo Seto 《Tetrahedron letters》1985,26(32):3845-3848
Feeding experiments with [2-3H3]acetate and [2-13C2H3]acetate in Thom No. 14 indicated that the hydrogen at C-2 in terrecyclic acid A is incorporated without migration from the precursor acetic acid; the results favour our group's earlier speculation for the cyclization to the tricyclic skeleton in the biosynthetic scheme. 相似文献
122.
DL-2-(4-2-Thienylcarbonyl)phenyl)propionic acid (suprofen) was rapidly absorbed in both sexes of rats, guinea pigs, and rabbits after oral administration. Blood levels after a single dose of 2 mg/kg 3H-suprofen in all the animals reached maxima within 15 min, and elimination of the 3H from blood was rapid; the radioactivity was mostly excreted in the urine and feces within 24 h after dosing. 相似文献
123.
Ayumi Yoshida Hitoshi Yamauchi Hideki Sakai Norimichi Kawashima Masahiko Abe 《Colloids and surfaces. B, Biointerfaces》1997,8(6):191-342
Molecular interactions between lipid bilayers (liposomes) and chondroitin sulfate C (CS), a water soluble polymer, have been investigated in terms of zeta-potential, particle size, microscopic-viscosity, microscopic-polarity of liposomes and permeability of calcein. Microscopic morphology is dramatically changed by the addition of CS to the positively charged liposomes (Pos.L), while it is not changed by the addition to uncharged liposomes (Unc.L) or negatively charged liposomes (Neg.L). The absolute value of the particle size of Pos.L increases with the addition of CS, while the zeta- potential of Pos.L decreases. Permeability of Pos.L decreases with an increase in the concentration of CS. Phase transition temperature of Pos.L is changed after the addition of CS. These values, however, are not changed for the other liposomes by the addition of CS. The results of gel filtration chromatography show that CS is absorbed on the Pos.L surface. Microscopic viscosity is also increased by the addition of CS to Pos.L due to the adsorption of CS. 相似文献
124.
Oki Michinori Toyofuku Yoshitaka Sakaue Tatsuya Hirose Takanori Asakura Mitsuhiro Morita Nobuhiro Toyota Shinji 《Russian Journal of Organic Chemistry》2003,39(4):542-553
X-ray crystallography of the ap-form of the 1-(9-fluorenyl)-2-(2-methyl-2-oxiranyl)naphthalene has revealed that the carbon atom of the oxirane which is connected to the naphthyl group in this compound is almost planar. The specific structural features of the epoxy ring in this compound are caused by sterical effects and by the presence of a -system in the immediate vicinity of the oxirane ring. Certain differences have been found also in reactivity of rotational isomers of 2-X-substituted 1-[1-(9-fluorenyl)-2-naphthyl]ethyl cations (X = O, S, Se). At X = O arose more deprotonation product from the -position of the oxygen than in reactions of sulfur and selenium-containing analogs. Reactions of epoxides with zinc chloride almost exclusively gave the corresponding aldehydes. 相似文献
125.
Chatani N Oshita M Tobisu M Ishii Y Murai S 《Journal of the American Chemical Society》2003,125(26):7812-7813
A GaCl3-catalyzed reaction of alpha,beta-unsaturated ketones with isocyanides leading to the formation of unsaturated lactone derivatives is described. This is the first example of the catalytic [4+1] cycloaddition of alpha,beta-unsaturated ketones and isocyanides. GaCl3 is an excellent catalyst due to its lower oxophilicity, which is desirable for all of the key steps, such as E/Z isomerization, cyclization, and deattachment from the products. 相似文献
126.
Bunichiro Yamada Shinji Tagashira Shuzo Aoki 《Journal of polymer science. Part A, Polymer chemistry》1994,32(14):2745-2754
The dimerization of methyl methacrylate, ethyl methacrylate, methacrylonitrile, and α-methylstyrene to 2-substituted-1-allylic compounds [CH2?C(X)CH2C(CH3)2X] (X = COOR, C6H5, or CN), and methyl α-ethylacrylate to a 3-substituted-2-allylic compound [CH3CH?C(COOCH3)CH2C(CH3)(C2H5) COOCH3] was carried out by catalytic chain transfer using benzylbis (dimethylglyoximato) (pyridine) cobalt (III). These dimers were then used as addition-fragmentation chain transfer agents in the polymerizations of methyl methacrylate and styrene at 800C or above. Cross-dimers from methacrylic ester-α-methylstyrene and methacrylonitrile-α-methylstyrene mixtures were similarly prepared. Except for those from methyl α-ethylacrylate and methacrylonitrile, all the dimers participated in the addition-fragmentation and the copolymerization to different extents. The dimer of methyl α-ethylacrylate was actually inactive during the styrene and methyl methacrylate polymerizations. The methacrylonitrile dimer was primarily incorporated in the polymer chain through copolymerization. Among the dimer and the cross-dimers from α-methylstyrene with the other monomers, those bearing the α-methylstyrene moiety in the α-substituent [CH2?C(X)CH2C(CH3)2C6H5, X?COOCH3, COOC2H5, and CN] are noted as highly reactive chain transfer agents. © 1994 John Wiley & Sons, Inc. 相似文献
127.
Identification and formation mechanism of individual degradation products in lithium‐ion batteries studied by liquid chromatography/electrospray ionization mass spectrometry and atmospheric solid analysis probe mass spectrometry
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130.
Rumiko Sakurai Kenichi Sakai Koichi Kodama Masanori Yamaura 《Tetrahedron: Asymmetry》2012,23(3-4):221-224
A useful key intermediate for the dipeptidyl peptidase-4 (DPP-4) inhibitor, 3-aminopiperidine 1, was successfully resolved with an enantiomerically pure resolving agent, N-tosyl-(S)-phenylalanine 2, to give both stereoisomers (R)-1 and (S)-1 as a less-soluble diastereomeric salt with (S)-2, via a dielectrically controlled resolution (DCR) phenomenon. 相似文献