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121.
(±)-Tryptoquivaline G was formally synthesized through shortened steps from tryptophan, in which oxidation with thallium(III) trinitrate(TTN) was effected at the crucial stage. The present work also constitutes the first synthesis of oxindole lactones carrying 2-alkyl quinazolinones. 相似文献
122.
Tomooka K Komine N Fujiki D Nakai T Yanagitsuru S 《Journal of the American Chemical Society》2005,127(35):12182-12183
Remarkably stable planar chirality was found in a nine-membered diallylic cyclic ether. Enantiomerically enriched ether was prepared by a kinetic resolution of a racemic one, which is valuable as a novel type of chiral building block. 相似文献
123.
Pressure effects on 1H chemical shifts and relaxation rates in organic solvents containing the nitroxide radical have been observed. 1H chemical shifts with pressure and pressure-broadenings for hydrogen bonding between proton-donor molecules and the nitroxide radical have been observed. 相似文献
124.
Norio Tsubokawa Shingo Ohshima Yasuo Sone Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》1987,25(3):935-943
The ring-opening transfer polymerization of spiro ortho esters (SOE) initiated by carbon black was investigated. In the absence of carbon black, no polymerization occurred at all. In the presence of channel black containing carboxyl group, the ring-opening transfer polymerization of SOE was initiated at 50-70°C. to give polyether ester, namely alternating copolymer of epoxide and lactone. The rate of polymerization of 1,4,6-trioxaspiro[4.4]nonane and 1,4,6-trioxaspiro[4.5]decane was considerably small compared with that of 1,4,6-trioxaspiro[4.6]undecane. The activation energy of the polymerization of 2-chloromethyl-1,4,6-trioxaspiro[4.6]undecane was estimated to be 6.0 kcal/mol. The initiating activity of carbon black increased with an increase in carboxyl group content of carbon black. Furnace black that contained no carboxyl group was unable to initiate the polymerization. Furthermore, the carbon black lost the initiating ability of the polymerization upon the blocking of carboxyl group on the surface by the treatment with potassium hydroxide or diazomethane. Based on these results, it was concluded that carboxyl group on carbon black plays an important role in the initiation. During the polymerization, a part of the polymer formed was grafted onto carbon black: the grafting ratio was 10–30%. The mechanisms of initiation and grafting were discussed. 相似文献
125.
Satoshi ObikaJyun-ichi Andoh Mayumi OnodaOsamu Nakagawa Akiko HirotoTomomi Sugimoto Takeshi Imanishi 《Tetrahedron letters》2003,44(28):5267-5270
A novel bridged nucleic acid monomer, 3′-amino-3′-deoxy-5-methyl-3′-N,4′-C-methyleneuridine, was successfully synthesized via a useful and convenient azetidine ring formation under Staudinger's conditions. A 1H NMR experiment and a PM3 calculation revealed that the sugar moiety of the novel bridged nucleic acid monomer, 3′-amino-3′,4′-BNA, was restricted to S-type conformation. 相似文献
126.
Takeshi Takeda Tomohiro ShonoKenji Ito Hironori SasakiAkira Tsubouchi 《Tetrahedron letters》2003,44(43):7897-7900
Aldehydes, ketones, esters and lactones are transformed into enol ethers or 1,2-dialkoxy-1-alkenes by treatment with organotitanium species prepared from alkoxymethyl chlorides and a titanocene(II) complex. 相似文献
127.
M Miyauchi R Endo K Watanabe Y Kawahara M Iwata I Kawamoto 《Chemical & pharmaceutical bulletin》1990,38(6):1587-1590
Acyloxyalkyl esters (2a-d), alkyloxycarbonyloxyalkyl esters (2e-g) and (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl ester (2h) of (5R,6S)-2-(2-fluoroethylthio)-6-[(1R)-1-hydroxyethyl]penem-3- carboxylic acid (1) were synthesized. Enhanced oral absorption was observed in mice reflecting increased lipophilicity, compared with the parent 1 itself. Among them, the ester 2h showed a prolonged plasma level and a large area under the blood concentration-time curve (AUC) in rats. These ester-type prodrugs of penem 1 in phosphate buffer (pH 6.86) were much more stable than those of cephalosporins which easily degraded via isomerization to delta 2 cephalosporins. 相似文献
128.
Terutaka Watanabe Takeshi Wada Masaaki Takehisa Sueo Machi 《Journal of polymer science. Part A, Polymer chemistry》1974,12(8):1619-1628
The heterogeneous polymerization of ethylene initiated by radiation in tert-butyl alcohol was studied. The polymerization was carried out in a 100-ml reactor at 25–100°C and pressures of 200–300 kg/cm2 in the presence of 50 ml of tert-butyl alcohol containing 7 wt-% water. The amounts of polymerized monomer, the average molecular weight of polymer formed, and the molecular weight distribution of polymer were measured at various stages of reaction and at various temperatures. The molecular weight distribution was found to be very much dependent on the reaction time and temperature. For the polymer formed at 50–60°C in the very early stages of reaction, the molecular weight distribution is unimodal, and in the intermediate stage a shoulder appears at a molecular weight higher than the first peak which increases as the polymerization proceeds; eventually a bimodal curve is formed. The bimodal distribution curves were analyzed to determine the fractions and average molecular weights of the each peak. On the basis of these data for the molecular weight distribution and kinetic behavior, a new scheme for the heterogeneous polymerization is proposed which indicates that the polymerization proceeds via propagating radicals in two different physical states, namely, loose and rigid states. 相似文献
129.
The C-12˜C-17 segment
of (+)-aplasmomycin (
) was synthesized stereoselectively starting from (−)-malic acid based on the stereoselective ketone reduction. 相似文献
130.
Kentaro Ageishi Takeshi Endo Makoto Okawara 《Journal of polymer science. Part A, Polymer chemistry》1981,19(5):1085-1090
The behavior of viologen polymer (P-V2+) as an electron transfer catalyst in the reaction of hydrogen generation was studied. In the photoirradiation system, which contains triethanolamine (TEA), Ru(bpy)3+3, and P-V2+, the amount of hydrogen evolution was less than methyl viologen (MV2+); P-V2+, however, was more effective in sodium dithionite as the electron donor and showed higher initial rates than MV2+. 相似文献