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Rearrangements Changing the Structure of a Sugar Skeleton

This chapter shows selected examples of the rearrangement of the sugar skeleton leading to the open-chain derivatives. [Pg.224]

FIGURE 10.13 Unexpected rearrangement of pyranopyrans that open a route to pentenyl  [Pg.225]

This observation opened a route to so-called pentenyl glycoside methodology [32, 33], which is now one of the most important methods of the creation of the glycosidic bond. [Pg.225]

FIGURE 10.14 Preparation of unsaturated sugars by Vasella procedure. [Pg.225]

FIGURE 10.15 Synthesis of complex polyhydroxylated products utilizing the VaseUa [Pg.226]


See other pages where Rearrangements Changing the Structure of a Sugar Skeleton is mentioned: [Pg.224]    [Pg.225]   


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A rearrangements

As sugars

Skeleton rearrangement

Skeleton structure

Structural change

Structural rearrangement

Structure change

Sugar structure

The Sugars

The skeleton

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