Abstract
By analysis of the products from the protolytic cleavage of methyl 3-(2,5-dialkoxy-2,5-dihydro-2-furyl)propionate (I) in the presence of mixed nucleophiles and investigation of their mutual transformations the main paths in the dissociation of the protonated molecule of (I), with the formation of both linear cleavage products (derivatives of 1,4-diketones and 4-ketopimelic acid) and furylcarbinol derivatives, were determined.
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Latvian Institute of Organic Synthesis. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 190–197, February, 1997.
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Lolya, D., Freimanis, Y., Gavar, M. et al. Protolytic cleavage of derivatives of 2,5-dimethoxy-2,5-dihydrofuran. Chem Heterocycl Compd 33, 164–170 (1997). https://doi.org/10.1007/BF02256757
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DOI: https://doi.org/10.1007/BF02256757