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• W2115677653 abstract "Macrocycles consisted of pyridine rings and acetylene bonds were prepared by Eglinton coupling from a tandem precursor bearing two terminal alkynyl groups. The composition of molecular size in the cyclized products changed by the reaction solvent. In pyridine, 9-meric and bigger macrocycles were obtained, while that of 6-mer was not. On the other hand, in pyridine/THF mixed solvent, the 6-mer was obtained as a major product." @default.
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• W2115677653 date "2010-12-08" @default.
• W2115677653 modified "2023-10-17" @default.
• W2115677653 title "Preparation of Ethynylpyridine Macrocycles by Oxidative Coupling of an Ethynylpyridine Trimer with Terminal Acetylenes" @default.
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• W2115677653 doi "https://doi.org/10.1021/jo101921e" @default.
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