Interconversible cis and trans Rotational Isomers of 1,8-Di (1-naphthyl) naphthalene
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概要
- 論文の詳細を見る
New stable cis and trans rotational isomers of 1,8-di (1-naphthyl) naphthalene were prepared by the Kharash-type Grignard cross-coupling of 1-naphthylmagnesium iodide and 1,8-diiodonaphthalene in the presence of N, N'-bis (1-methyl-3-oxobutylidene) ethylene-diaminatonickel (II). Thermoanalytical and proton magnetic resonance spectral studies indicated that both rotamers are stable in the solid state as well as in a solution, but are interconversible at temperatures above their melting points. A convenient method, obtaining pure trans rotamer from the equilibrium mixture of both rotamers, is also presented.
- 社団法人日本薬学会の論文
- 1981-07-25
著者
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小笹 茂
Kyoto Pharmaceutical University
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藤岡 靖弘
Kyoto Pharmaceutical University
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伊夫伎 英一
Kyoto Pharmaceutical University
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水谷 弘
Kyoto College of Pharmacy
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