Sugar synthesis catalyst

Another example of the ability of proteinogenic amino acids, small peptides, and amines to catalyse the formation of new C-C bonds has been demonstrated by Weber and Pizzarello they were able to carry out model reactions for the stereospecific synthesis of sugars (tetroses) using homochiral L-dipeptides. The authors achieved a D-enantiomeric excess (ee) of more than 80% using L-Val-L-Val as the peptide catalyst in sugar synthesis (in particular D-erythrose) via self-condensation of glycol aldehyde. 

Sorbitol is a sweetener often substituted for cane sugar because it is better tolerated by dia betics It IS also an intermediate in the commercial synthesis of vitamin C Sorbitol is prepared by high pressure hydrogenation of glucose over a nickel catalyst What is the structure (including stereochemistry) of sorbitoP... 

The reaction is used for the chain extension of aldoses in the synthesis of new or unusual sugars In this case the starting material l arabinose is an abundant natural product and possesses the correct configurations at its three chirality centers for elaboration to the relatively rare l enantiomers of glucose and mannose After cyanohydrin formation the cyano groups are converted to aldehyde functions by hydrogenation m aqueous solution Under these conditions —C=N is reduced to —CH=NH and hydrolyzes rapidly to —CH=0 Use of a poisoned palladium on barium sulfate catalyst prevents further reduction to the alditols... 

In bioprocesses, the feedstocks required to grow the catalysts and produce the chemical renewable are generally renewable resources, such as sugar from crops. Conversely, purely feedstocks chemical synthesis relies largely on non-renewable resources such as oil, coal and natural gas. It follows that as non-renewable resources dwindle, it is likely that biotechnology will become increasingly important to the chemical industry. 

Two-step synthesis of sugar-containing polyesters by lipase CA catalyst was reported (Scheme 13)." Lipase CA catalyzed the condensation of sucrose with an excess of divinyl adipate to produce sucrose 6,6 -O-divinyl adipate, which was reacted with a,oo-alkylene diols by the same catalyst, yielding polyesters containing a sucrose unit in the main chain. This method conveniently affords... 

A. P. Rauter, F. Ramoa-Ribeiro, A. C. Fernandes, and J. A. Figueiredo, A new method of acetonation with the zeolite HY as catalyst. Synthesis of O-isopro-pylidene sugar derivatives, Tetrahedron, 51 (1995) 6529-6540. 

V. K. Rajput and B. Mukhopadhyay, Sulfuric acid immobilized on silica An effcient reusable catalyst for the synthesis of O-isopropylidene sugar derivatives, Tetrahedron Lett., 47 (2006) 5939-5941. 

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