Abstract:
1,5-Diphenylpentane-1,5-dione reacts (50 mol% KOH in DMSO, 70°C, 3h) with phenylacetylene in a domino manner to afford 3-benzoyl-2-benzyl-1-phenylcyclopenten-1-ol and its debenzoylated derivative in 66 and 25% yields, respectively.
Bibliographic databases:
Document Type:
Article
Language: English
Citation:
B. A. Trofimov, E. Yu. Schmidt, I. A. Bidusenko, N. A. Cherimichkina, “Domino assembly of functionalized cyclopentenols from 1,5-diphenylpentane-1,5-dione and phenylacetylene in the KOH/DMSO suspension”, Mendeleev Commun., 25:1 (2015), 17–18
Linking options:
https://www.mathnet.ru/eng/mendc2284
https://www.mathnet.ru/eng/mendc/v25/i1/p17
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