共查询到20条相似文献,搜索用时 15 毫秒
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Rodney L. Willer Robson F. Storey Mark Frisch Jeffery R. Deschamps 《Journal of heterocyclic chemistry》2012,49(1):227-231
The crystal structures of the two compounds reported to be 4‐aminofurazan‐3‐carboxylic acid have been determined. The compound reported by Sheremetev et al. (J Heterocycl Chem 2005, 42, 519) is the actual 4‐aminofurazan‐3‐carboxylic acid. The compound reported by Meyer (Org Prep Proced Int 2004, 36, 361) is the interesting complex formed from a molecule of the acid and a molecule of the potassium salt of the acid. J. Heterocyclic Chem., (2012). 相似文献
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Shujiang Tu Fang Fang Songlei Zhu Tuanjie Li Xiaojing Zhang Qiya Zhuang Shuijun Ji Yong Zhang 《Journal of heterocyclic chemistry》2005,42(1):29-32
The synthesis of bifunctional pyridine and quinolione derivatives were investigated using terephthalic and isophthalic aldehydes as a precursor. The reaction proceeds under microwave irradiation with good yield (70–92%) and short reaction time (7–9 min.). We provide a rapid and efficient method of synthesizing a range of bifunctional monocyclic and bicyclic products related to 1,4‐dihydropyridines (1,4‐DHPs). 相似文献
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Dr. Yu Kitazawa Mamoru Watanabe Yui Masumoto Mai Otsuka Dr. Kazunori Miyamoto Dr. Atsuya Muranaka Dr. Daisuke Hashizume Dr. Ryo Takita Prof. Dr. Masanobu Uchiyama 《Angewandte Chemie (International ed. in English)》2018,57(6):1501-1504
We designed, synthesized, and characterized two types of dimeric forms of monocarba‐closo‐dodecaborate, namely, a “dumbbell”‐shaped dianion having a C?C bond and a “clackers”‐shaped monoanion having an iodonium linker. The unique architectures of these anionic molecules were established by X‐ray analysis. Spectroscopic analysis, DFT calculations, and reactivity experiments revealed high anionic and chemical stability of both anions, which are crucial properties for weakly coordinating anions. 相似文献
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A. R. Suresh Babu R. Raghunathan G. Gayatri G. Narahari Sastry 《Journal of heterocyclic chemistry》2006,43(6):1467-1472
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《Nachrichten aus der Chemie》2012,60(12):1234-1235
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Hideyuki Higashimura Kiyoshi Fujisawa Masaaki Kubota Shiro Kobayashi 《Journal of polymer science. Part A, Polymer chemistry》2005,43(9):1955-1962
“Radical‐controlled” oxidative polymerization of phenol (p‐1) by (1,4,7‐triisopropyl‐1,4,7‐triazacyclononane)copper(II) catalyst was performed and compared with that of 4‐phenoxyphenol (p‐2) in detail. Although the coupling selectivity for p‐1 seemed to be controlled by the catalyst, the C? C coupling, which was excluded completely for p‐2, occurred to some extent. The initial reaction rate of p‐1 was much smaller than that of p‐2, leading to the difference of polymerization behavior between p‐1 and p‐2. The rate‐determining step would be the coupling of controlled radicals species from the ESR measurement of the reaction mixture. The polymer resulting from p‐1 consisted mainly of phenylene oxide units, but had no crystallinity in contrast to the crystalline polymer from p‐2. However, the present polymer showed the highest thermal stability in the polymers obtained by oxidative polymerization of p‐1. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1955–1962, 2005 相似文献
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