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Mendeleev Communications, 2001, Volume 11, Issue 2, Pages 82–83
DOI: https://doi.org/10.1070/MC2001v011n02ABEH001390 (Mi mendc4229) 		 
This article is cited in 2 scientific papers (total in 2 papers)

Cyclization of 5-(2-chloroethoxy)-1,5-dihydro-2H-pyrrol-2-ones

K. V. Nikitina, N. P. Andryukhovaa, E. K. Ryub

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b Bioorganic Science Division, Korean Research Institute of Chemical Technology, Taejon, Korea
Full-text PDF (86 kB) Citations (2)
DOI: https://doi.org/10.1070/MC2001v011n02ABEH001390
Abstract: The intramolecular cyclization of substituted 5-(2-chloroethoxy)-1,5-dihydro-2H-pyrrol-2-ones in the presence of lithium diisopropylamide hexamethylphosphoramide in tetrahydrofuran gave tetrahydropyrano[2,3-b]pyrrol-6(2H)-ones and 3,4-dihydro-2H-pyrrolo-[2,1-b][1,3]oxazin-6(8aH)-ones in moderate to good yields.
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Document Type: Article
Language: English


Citation: K. V. Nikitin, N. P. Andryukhova, E. K. Ryu, “Cyclization of 5-(2-chloroethoxy)-1,5-dihydro-2H-pyrrol-2-ones”, Mendeleev Commun., 11:2 (2001), 82–83
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    • This publication is cited in the following 2 articles:
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