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71.
Kuroda N Hattori T Fujioka Y Cork DG Kitada C Sugawara T 《Chemical & pharmaceutical bulletin》2001,49(9):1147-1154
An in-house developed automated synthesis suite was used to prepare a library of 72 tetrapeptide derivatives, the starting materials for pharmaceutically attractive pentapeptides, employing a convergent strategy. An initial set of 18 dipeptides were synthesized on a large-scale (100-1000 g) using automated synthesis workstations, and then 72 tetrapeptides were synthesized on a medium scale (5-10 g) using an automated system. Each di- or tetrapeptide was prepared in a single operating cycle using a modified methanesulfonic acid method, then a sub-library of 56 pentapeptides were synthesized in parallel, on a small-scale (100 mg-1 g) using a robotic workstation. 相似文献
72.
Synthesis of two naturally occurring 3-methyl-2,5-dihydro-1-benzoxepin carboxylic acids 总被引:1,自引:0,他引:1
[structures: see text] Two naturally occurring 3-methyl-2,5-dihydro-1-benzoxepin carboxylic acids, 6-hydroxy-3-methyl-8-(phenylethyl)-2,5-dihydro-1-benzoxepin-9-carboxylic acid (radulanin E) (1) and 9-hydroxy-3-methyl-2,5-dihydro-1-benzoxepin-7-carboxylic acid (2), were synthesized using Stille coupling followed by Mitsunobu cyclization. 相似文献
73.
The induced circular dichroism (ICD) spectra of the inclusion complexes of maleimide, phthalimide, and naphthalene‐2,3‐dicarboximide with β‐ or γ‐cyclodextrin (CDx) have been measured. The structure of the CDx inclusion complexes are interpreted by the signs and shapes of ICD spectra compared with the results of PPP calculations. In maleimide and naphthalene‐2,3‐dicarboximide, the ICD spectra of the β‐CDx inclusion complex are very similar to those of the γ‐CDx inclusion complex in spite of the differences in dimensions between the cavity of β‐CDx and that of γ‐CDx. In phthalimide, the ICD spectra of the β‐CDx inclusion complex are very different from those of the γ‐CDx inclusion complex. The split‐type ICD bands at 220–235 nm show that the dimer of phthalimide is formed in the presence of β‐CDx. 相似文献
74.
Hidefumi Makabe Yasunao Hattori Hiroyuki Konno Hideto Miyoshi Takayuki Oritani 《Tetrahedron》2004,60(47):10651-10657
A convergent total synthesis of cis-solamin (1a) and its diastereomer (1b) was accomplished. A key reaction of this approach was the use of VO(acac)2-catalyzed diastereoselective epoxidation of (Z)-bis-homoallylic alcohol 3 followed by spontaneous cyclization for the cis-THF ring formation. By comparison of the optical rotation of the two possible diastereomers, it is suggested that the absolute configuration of natural cis-solamin is 1a. Inhibitory action of synthetic 1a and 1b with bovine heart mitochondrial complex I are reported. 相似文献
75.
Novel Lewis-base ionic liquids replacing typical anions 总被引:1,自引:0,他引:1
Masahiro Yoshizawa-Fujita Katarina Johansson Douglas R. MacFarlane 《Tetrahedron letters》2006,47(16):2755-2758
We have synthesized two kinds of new Lewis-base ionic liquids (ILs); one is based on the relatively strong Lewis basic acetate anion, and the other is a salt composed of a mono-alkylated diamine such that the Lewis base site is incorporated in the cation. 1-Octyl-4-aza-1-azonia-bicyclo[2.2.2]octane bis(trifluoromethanesulfonyl)amide, [C8dabco]TFSA, and N-butyl-N-methylpyrrolidinium acetate, [p1,4]OAc, melted into fluid liquids at 26 and 81 °C, respectively. The thermal decomposition of [p1,4]OAc started at around 150 °C, whereas the thermal stability of [C8dabco]TFSA was almost equal to that of typical TFSA-based ILs in spite of the Lewis base site. This suggests that if the Lewis base site is incorporated into the cation the IL can maintain higher thermal stability. In addition, as a further result of the presence of the basic nitrogen, [C8dabco]TFSA can dissolve hydrated Cu(NO3)2 whereas the other TFSA-based ILs cannot. 相似文献
76.
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78.
Changes in the fluorescence intensity of polyanions bearing 4-acryloylbenzo-18-crown-6 units on the addition of cations were studied in a mixed solvent of methanol and water at 30°C. The sensitivity of the change in fluorescence intensities of the polymers toward cations was strongly enhanced compared to that of the corresponding model compound. When alkali metal cations were added, the fluorescence intensity of the polymers decreased in the orders Li+>Na+>Cs+>Rb+>K+ in a methanol-water (19) mixture and Li+>Na+>Rb+>K+Cs+ in a methanol-water (91) mixture. Alkaline earth metal cations and alkylamine hydrochlorides decreased the fluorescence intensity of the polymers in a methanol-water (19) mixture. The cation-dependent decrease in the fluorescence intensity of the polymers was affected by the water fraction in a mixed solvent of methanol and water. 相似文献
79.
Glycyrrhetic acid (GA), aglycone of glycyrrhizin (GL), inhibited potently (I50 = 7 x 10(-6) M) and non-competitively the activity of NAD(P)+-linked 3 alpha-hydroxysteroid dehydrogenase of rat liver cytosol. The inhibition was slightly weaker than that of indomethacin, a potent anti-inflammatory agent, but stronger than that of dexamethasone, another anti-inflammatory agent. GL, GA monoglucuronide, and 3-epi-glycyrrhetic acid also inhibited this enzyme activity, but did so less effectively (I50 = 5-8 x 10(-5) M). Carbenoxolone (GA 3-hemisuccinate) and 3-keto-glycyrrhetic acid showed potent inhibitory effects similar to GA, and 18 alpha-GA showed the most powerful inhibition of the activity. 相似文献
80.
Kondo F Saito H Hayashi R Onda H Kobayashi S Matsumoto M Suzuki M Ito Y Oka H Nakanishi T Shimizu A 《The Analyst》2003,128(11):1360-1364
We developed a rapid and reliable identification method for Shiga toxins in Shiga toxin-producing Escherichia coli (STEC) using immunoprecipitation and high-performance liquid chromatography-electrospray ionization mass spectrometry (HPLC-ESI-MS). Polyclonal antisera specific for Shiga toxin 1 (Stx1) and Shiga toxin 2 (Stx2) were raised in rabbits so as to be used for the immunoprecipitation. The immunoprecipitaion was carried out by mixing sample solutions with 50 microl each of the antisera to Stx1 and Stx2 followed by allowing the mixed solutions to stand for 30 min. The quantity required to obtain the immunoprecipitate was more than 0.5 microg of Shiga toxins. HPLC-ESI-MS analysis of the resulting immunoprecipitates provided accurate molecular weight information on Shiga toxins, leading to direct evidence for the presence of these toxins. It requires at most two days to perform our procedure from toxin extraction to measurement of HPLC-ESI-MS whereas the previous method using isolation procedures required about two weeks to complete. The usefulness of the present method has been demonstrated by identifying Stx1, Stx2 and a variant of Stx2 (Stx2e) in the immunoprecipitates prepared from STEC strains. 相似文献