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- W2040405236 abstract "A family of furoquinolines were efficiently obtained through a tandem acetalization/cycloisomerization process catalyzed by (5 mol%) silver imidazolate polymer and triphenylphosphine, and diversity was brought by the use of 7 different alcohol groups. From these furoquinolines, 3 examples of reduced derivatives could be obtained (d.r. up to 94 : 6), 10 different spiroketal derivatives by hetero-Diels–Alder reaction (d.r. up to 20 : 1), 8 hetero-[5,5]-spirocycles by cycloaddition with dibromoformaldoxime (d.r. up to 86 : 14) and finally 6 hetero-[5,6]-spirocycles by [4 + 2] cycloaddition with ethyl 3-bromo-2-(hydroxyimino)propanoate (d.r. up to 90 : 10)." @default.
- W2040405236 created "2016-06-24" @default.
- W2040405236 creator A5037291441 @default.
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- W2040405236 creator A5065024340 @default.
- W2040405236 creator A5066035534 @default.
- W2040405236 creator A5010754802 @default.
- W2040405236 date "2011-01-01" @default.
- W2040405236 modified "2023-10-03" @default.
- W2040405236 title "Synthesis and reactivity of furoquinolines bearing an external methylene-bond: access to reduced and spirocyclic structures" @default.
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- W2040405236 doi "https://doi.org/10.1039/c1ob05354j" @default.
- W2040405236 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21544305" @default.
- W2040405236 hasPublicationYear "2011" @default.
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