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641.
Rui Tamura Hiroki Takahashi Hideyuki Miura Zsolt Lepp Yoshitaka Nakajima Ken Hirotsu 《Supramolecular chemistry》2013,25(1):71-78
Abstract The crystal structures of (±)-[2-[4-(3-ethoxy-2-hydroxypropoxy)phenylcarbamoyl]ethyl] trimethylammonium p-chlorobenzenesulfonate [(±)-NCMe3] and its terminal methoxy derivative, (±)-NCMe3-OMe, are compared. The former racemate exhibited the phenomenon of Preferential Enrichment, whereas the latter failed to do so. Crystal data, (±)-NCMe3: CuKα radiation, space group P 1, Z = 2, a = 9.848(5), b = 14.823(3), c = 9.147(1) Å, α = 97.81(1), β = 92.68(3), γ = 105.92(2)°, D calc = 1.355 g/cm3, R = 0.056 for 3213 observed reflections; (±)-NCMe3-OMe: CuKα radiation, space group P 1, Z = 2, a = 11.350(1), b = 14.568(2), c = 8.2981(4) Å, α = 94.346(7), β = 112.376(5), γ = 78.622(9)°, D calc = 1.343 g/cm3, R = 0.069 for 1519 observed reflections. 相似文献
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Ken-ichi Ito Yoshitaka Shigeru Masahiro Tsunooka 《Macromolecular rapid communications》1996,17(4):203-207
Films of polymers bearing pendant acyloxyimino (AOI) groups become insoluble when irradiated by ultraviolet light in the presence of p-benzoquinone. Post-heating of these films after irradiation also induces further the insolubilization. In the photocrosslinking, it is deduced that p-benzoquinone serves not only as sensitizer for the decomposition of AOI groups but also as crosslinker during the photo-irradiation and heating after irradiation. 相似文献
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Jun'ichi Uenishi Mitsuhiro Motoyama Yoshitaka Nishiyama Yuichi Hirota Yuki Kubo Haruo Akashi 《Heteroatom Chemistry》1994,5(1):51-60
Stereospecific ring openings of optically active 2,3-epoxy alcohols were performed by the reaction of 1 , 3 , 5 , and 7 with carbon disulfide and sodium hydride to give the five-membered xanthates 2 , 4 , 6 , and 8 . Both enantiomers of 2-mercapto-1,3-diol triacetates, 11 and 14 , were derived from 4 and 6 , respectively. The ring opening reaction proceeded at −78°C to −30°C, and the yields were around 80%. However, at a higher temperature between 0°C to room temperature, a complicated reaction took place and led to the formation of two isomers of the cyclic thiol carbonates 15 and 16 from 1 or 5 . These processes were also stereospecific, and mechanisms have been proposed. In the case of the 3,4-epoxy alcohol 20 , the epoxide ring opening gave the six-membered xanthate 21 stereospecifically. 相似文献