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1.
Masahiro Kurokawa Hidemasa Yamaguchi Yuji Minoura 《Journal of polymer science. Part A, Polymer chemistry》1979,17(2):485-492
l-Menthyl vinyl ether (l-MVE) was homopolymerized and copolymerized with the monomers indene (IN) and acenaphthylene (ANp) by BF3OEt2 as a catalyst. The chiral menthyl substituent was cloven from the homopolymers and copolymers using dry-hydrogen bromide gas. After the removal of optically active menthyl group, poly(vinyl alcohol) (PVA) from l-MVE homopolymer was optically inactive, and copolymers (VA-IN, VA-ANp) from l-MVE-IN and l-MVE-ANp copolymers were still optically active. Hence, in the case of l-MVE homopolymer, it was concluded that asymmetric induction in the polymer main chain can only produce pseudoasymmetry. In the case of l-MVE-IN and l-MVE-ANp copolymers, it was found that asymmetric induction proceeded in the copolymer main chain and was caused by the influence of chiral menthyl group. 相似文献
2.
Masahiro Kurokawa Yuji Minoura 《Journal of polymer science. Part A, Polymer chemistry》1979,17(10):3297-3305
The copolymerizations of l-menthyl vinyl ether (l-MVE) with the monomers vinylene carbonate (VCA) and indene (IN) were carried out in benzene with azobisisobutyronitrile (AIBN) as an initiator to obtain optically active copolymers. The optically active l-menthyl residue from the copolymer main chain was removed using dry hydrogen bromide gas. After the ether cleavage reaction, the copolymers prepared (VA–VCA and VA–IN) were still optically active, and hence it was found that asymmetric induction had taken place in the copolymer main chain. The optical rotatory dispersion (ORD) and circular dichroism (CD) data of the original and ether-cloven copolymers were also determined. 相似文献
3.
Vilsmeier–Haack‐type cyclization of 1H‐indole‐4‐propanoic acid derivatives was examined as model construction for the A–B–C ring system of lysergic acid ( 1 ). Smooth cyclization from the 4 position of 1H‐indole to the 3 position was achieved by Vilsmeier–Haack reaction in the presence of K2CO3 in MeCN, and the best substrate was found to be the N,N‐dimethylcarboxamide 9 (Table 1). The modified method can be successfully applied to an α‐amino acid derivative protected with an N‐acetyl function, i.e., to 27 (Table 2); however, loss of optical purity was observed in the cyclization when a chiral substrate (S)‐ 27 was used (Scheme 5). On the other hand, the intramolecular Pummerer reaction of the corresponding sulfoxide 20 afforded an S‐containing tricyclic system 22 , which was formed by a cyclization to the 5 position (Scheme 3). 相似文献
4.
Reaction of β-cyclodextrin (β-CD) with CuCl2 in neutral aqueous solutions gave a stable molecular complex without any side-arm support. The X-ray crystallographic analysis clarified that the copper ion was located at the bottom of the primary-hydroxy side as a CuCl2(H2O)2 form. Hydrogen bonds were found between the Cl and H2O ligands and β-CD hydroxy and ether groups. The copper ion is axially coordinated with a hydroxy group of a neighboring β-CD molecule, giving a one-dimensional β-CD/CuCl2 array. 相似文献
5.
Jun Iwabuchi Takashi Kurokawa Zejian Gou Akira Hasegawa 《Journal of carbohydrate chemistry》2013,32(3):605-616
Abstract Benzyl 2,3-anhydro-4-azido-4-deoxy-α-L-ribopyranoside (7), an intermediate for the synthesis of Prumycin was synthesized in 72% yield in seven steps from D-arabinose. Ammonolysis of 7 followed by N-protection with the benzyloxycarbonyl group gave benzyl 4-azido-2-(benzyloxycarbonyl)amino-2,4-dideoxy-α-L-arabinopyranoside (8), which was easily converted to Prumycin. 相似文献
6.
Yoshinori Tominaga Yoshihide Shiroshita Tomohiko Kurokawa Hiromi Gotou Yoshiro Matsuda Akira Hosomi 《Journal of heterocyclic chemistry》1989,26(2):477-487
The reaction of 1-ethoxycarbonylmethylpyridinium bromides 5a-k with nitro ketene dithioacetal, 1,1-bis-(methylthio)-2-nitroethylene ( 2 ), in the presence of triethylamine in ethanol gave the desired ethyl 2-methyl-thioindolizine-3-carboxylates 3a-k in good yields, along with ethyl 2-methylthio-1-nitroindolizine-3-carboxyl-ates 4a-d . Deesterification of 3 using sodium hydroxide in methanol followed by treatment with polyphosphoric acid gave the corresponding 2-methylthioindolizines 5a-d in good yields. The desulfurization of 5 with Raney-nickel in ethanol occurs smoothly to give the 1,2,3-unsubstituted indolizines 6a-c (a , parent indolizine; b , 8-methylindolzine; c , 6,8-dimethylindolizine). Similarly, pyrrolo[2,1-a]isoquinoline ( 19 ) was also synthesized. These indolizine and pyrrolo[1,2-a]isoquinoline derivatives were allowed to react with dimethyl acetylene to give the corresponding cycl[3.2.2]azine and benzo[g]cycl[3.2.2]azine derivatives in good results. 相似文献
7.
S. Ota S. Shimoura H. Iwasaki M. Kurokawa S. Michimasa N. Aoi H. Baba K. Demichi Z. Elekes T. Fukuchi T. Gomi S. Kanno S. Kubono K. Kurita H. Hasegawa E. Ideguchi N. Iwasa Y.U. Matsuyama K.L. Yurkewicz T. Minemura T. Motobayashi T. Murakami M. Notani A. Odahara A. Saito H. Sakurai E. Takeshita S. Takeuchi M. Tamaki T. Teranishi Y. Yanagisawa K. Yamada M. Ishihara 《Physics letters. [Part B]》2008
8.
Tasuku Nakajima Takayuki Kurokawa Hidemitsu Furukawa Qiu Ming Yu Yoshimi Tanaka Yoshihito Osada Jian Ping Gong 《高分子科学》1996,(1):1-9
Living tissues work with fantastic functions in soft and wet gel-like state. Thus, hydrogels have attracted much attention as excellent soft & wet materials, suitable for making artificial organs for medical treatments.However, conventional hydrogels are mechanically too weak for practical uses. We have created double network (DN) hydrogels with extremely high mechanical strength in order to overcome this problem. DN gels are interpenetrating network (IPN) hydrogels consisting of rigid polyelectrolyte and soft neutral polymer. Their excellent mechanical properties cannot be explained by the standard fracture theories. In this paper, we discuss about the toughening mechanism of DN gels in accordance with their characteristic behavior, such as large hysteresis and necking phenomenon. We also describe the results on tissue engineering application of DN gels. 相似文献
9.
Sayoko Nagashima Shota Furukawa Satoshi Kamiguchi Ryu Kajio Hiroshi Nagashima Aritomo Yamaguchi Masayuki Shirai Hideki Kurokawa Teiji Chihara 《Journal of Cluster Science》2014,25(5):1203-1224
A series of molecular rhenium sulfide clusters [Re6S8(OH)6?n (H2O) n ](4?n)? (n = 0, 2, 4, 6) catalyze dehydrogenation of alcohols, and hydrogenation of ketones and olefins in a hydrogen stream at 350 °C. The catalytic activities of the dianionic and neutral clusters (n = 2, 4) are lower than those of tetraanionic and dicationic clusters (n = 0, 6) for all the reactions. When 1,4-butanediol is allowed to react over K4[Re6S8(OH)6], dehydrogenation proceeds to yield 2-hydroxytetrahydrofuran and successively γ-butyrolactone above 300 °C. Over [Re6S8(H2O)6]SO4 dehydration proceeds to yield tetrahydrofuran above 250 °C. The thermal activation mechanisms of these clusters were studied by powder X-ray diffraction analyses, Raman spectrometry, extended X-ray absorption fine structure spectrometry, thermogravimetry, and differential thermal analyses. The catalytically active site of K4[Re6S8(OH)6] is an uncoordinated metal site (Lewis acid site) developed by the loss of a water molecule from two hydroxo ligands. The active site of [Re6S8(H2O)6]SO4 is a Brønsted acid site; the anhydrous aqua cluster dication disproportionates to a hydroxo cluster monocation and a proton. Both of the octahedral cluster frameworks are retained up to 500 °C. 相似文献
10.
Saya Nakabayashi Katsunori Nagano Makoto Nakamura Junya Togawa Asami Kurokawa 《Adsorption》2011,17(4):675-686
The aim of this study is the development of a new adsorbent for the desiccant material which can be regenerated by the domestic
exhaust heat by using natural mesoporous material, Wakkanai siliceous shale. To improve this shale’s performance to adsorb/desorb
the water vapor, lithium chloride, calcium chloride or sodium chloride was supported into the mesopores by impregnating with
each chloride solution. Especially sodium chloride was effective to increase the water vapor adsorption amount 5–7 times of
that of natural shale in the relative humidity range from 50 to 70%. Moreover, the appropriate impregnating concentrations
were determined as 5wt% from the relationship between the maximum water vapor adsorption amount and the mesopore volume. Based
on these results, a new desiccant filter has been developed by impregnated original paper with lithium chloride and sodium
chloride. This paper contained shale powder in the synthetic fibers. The dehumidification performance of this filter was evaluated
under the simulated summer condition in Tokyo. From the cyclic adsorption/regeneration test, this shale and chlorides filter
could adsorb and desorb 60 g/h water vapor repeatedly at the regeneration temperature of 40°C. On the other hand, a silica
gel filter and a zeolite filter adsorbed and desorbed only 10 g/h and 25 g/h, respectively. These results suggested that the
shale impregnated with the chlorides has the best dehumidification ability as a new desiccant material. Further, the desiccant
filter made from the shale will achieve the effective use of the low temperature exhaust heat. 相似文献