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5-Arylidene Derivatives of Meldrum’s Acid as Synthons in Pyrano[4,3-b]pyran Synthesis

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Summary.

The reactions of 5-arylidene derivatives of Meldrum’s acid with ethyl vinyl ether or N-vinyl-2-oxazolidinone yielded trans-trans-(2,4:4,7)-pyrano[4,3-b]pyrans, cis-trans-(2,4:4,7)-pyrano[4,3-b]pyrans, or diastereoisomeric mixtures of pyrano[4,3-b]pyrans and reactions with 3,4-dihydro-2H-pyran afforded Michael adducts. The reactions of 5-arylidene derivatives of Meldrum’s acid with cyanoacetic acid derivatives do not provide appropriate pyrans.

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Authors and Affiliations

  1. Department of Organic Chemistry, Jagiellonian University, Kraków, Poland

    Aleksandra Pałasz, Katarzyna Jelska & Monika Ożóg

  2. Regional Laboratory, Jagiellonian University, Kraków, Poland

    Paweł Serda

Authors
  1. Aleksandra Pałasz
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  2. Katarzyna Jelska
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  3. Monika Ożóg
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  4. Paweł Serda
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Correspondence to Aleksandra Pałasz.

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Pałasz, A., Jelska, K., Ożóg, M. et al. 5-Arylidene Derivatives of Meldrum’s Acid as Synthons in Pyrano[4,3-b]pyran Synthesis. Monatsh. Chem. 138, 481–488 (2007). https://doi.org/10.1007/s00706-007-0622-5

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  • DOI: https://doi.org/10.1007/s00706-007-0622-5

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