Synthetic study directed toward novel multi-linked heterocycles
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概要
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2-Amino-4-(1-methylindol-3-yl)thiazole (11c) has a characteristic nucleophilic nature at the 5-position and add to the 4-position of acetylpyridinium acetate (13) producing 2-acetylamino-5-(1-acetyl-1,4-dihydropyridin-4-yl)-4-(1-methylindol-3-yl) thiazole (1c). Its structure was established by X-ray single crystallographic analysis. Applying the results, simple syntheses of the related tris- (1a-b and 2-8) and tetrakis-linked heterocycles (9) were achieved.
- 日本複素環化学研究所の論文
- 1997-00-00
日本複素環化学研究所 | 論文
- Reactions of 2-Triphenylphosphoimino-1-azaazulenes with Aryl Isocyanates and Aryl Isothiocyanates
- Synthesis and some reactions of 11-azacyclohept[a]azulen-3(3H)-ones and evaluation of their cytotoxic activity against HeLa S3 cells
- Palladium-catalyzed heteroarylamination of ethyl 2-chloro-1-azaazulene-3-carboxylate and annulation of heteroarylamino-1-azaazulenes
- Synthesis of [poly(2-pyridyl)-substituted]-1-azaazulenes
- Heteroarylamination and heteroarylsulfidation of 2-chloro-1-azaazulenes