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1.6- anhydro-4-5-benzyl-4-thio preparation

Reaction of benzyl a-D-glucopyranosyl cyclic sulfate 44 or benzyl a-D-galactopyranosyl cyclic sulfate 45 with 1,4-anhydro-2,3,5-tri-0-benzyl-4-thio-D-arabinol 46, followed by debenzylation and reduction, gave novel sulfonium sulfate derivatives 47a and 47b, respectively, which were used to prepare homologs of salacinol 48, a natural human maltase glucoamylase inhibitor, as lead candidates for the treatment of type 2 diabetes (Scheme 3) <2006JOC1111>. [Pg.853]

See other pages where 1.6- anhydro-4-5-benzyl-4-thio preparation is mentioned: [Pg.131] [Pg.225] [Pg.136] [Pg.140] [Pg.33] [Pg.283]

See also in sourсe #XX -- [ Pg.34 , Pg.136 ]

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1,6-anhydro 6-thio

1.6- anhydro preparation

1.6- anhydro-4-5-benzyl-4-thio

2 -thio-, preparation

Benzyl preparation