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Hydroxymethylation of furan and its derivatives in the presence of cation-exchange resins

โœ Scribed by I. Iovel; Yu. Goldberg; M. Shymanska


Publisher
Elsevier Science
Year
1989
Weight
811 KB
Volume
57
Category
Article
ISSN
0304-5102

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Alkylation of furan, thiophene, and pyrr
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The corresponding 2-furylhetarylmethanes were obtained by the reaction of furan, thiophene, or pyrrole with furfuryl alcohol in the presence of the strongly acidic Amberlyst 15 cation-exchange resin in the H + form. The alkylation of furan and thiophene takes place regiospecifically in the 2position

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