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Furandiols, tetrahydro

B. Solvolysis of Phosphoric Acid Derivatives.—Interest continues in neighbouring-group participation in the solvolysis of phosphate esters. As a potential model compound for investigating the mechanism of ribo-nuclease action, the phenyl hydrogen phosphate ester of c/j-3,4-tetrahydro-furandiol (24) has been the subject of a detailed study. Above (and probably also below) pH 4 hydrolysis gives solely the cyclic phosphate (25)... [Pg.100]

Tetrahydro-3,4-furandiol, T-24 Tetrahydro-2-furanmethanol, T-25 N-(Tetrahydro-3-furanyl)adenosine, T-13 A-(3-Tetrahydrofuranyl)-6-aminopurine riboside, T-13 Tetrahydrofurfuryl acrylate, T-25 Tetrahydrofurfuryl alcohol, T-25 Tetrahydrofurfuryl butyrate, T-25 Tetrahydrofurfuryl cinnamate, T-25 Tetrahydrofuro[3,2-6]furan-3,6-dione, D-756... [Pg.1109]

See other pages where Furandiols, tetrahydro is mentioned: [Pg.582]    [Pg.1607]    [Pg.582]    [Pg.1607]    [Pg.142]    [Pg.53]    [Pg.54]    [Pg.903]    [Pg.903]   
See also in sourсe #XX -- [ Pg.623 ]



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