New explortion of 14215-68-0

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 14215-68-0 is helpful to your research., Application In Synthesis of N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.14215-68-0, Name is N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide, molecular formula is C8H15NO6. In a Article£¬once mentioned of 14215-68-0, Application In Synthesis of N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide

Decarbonylation of Unprotected Aldose Sugars by Chlorotris(triphenylphosphine)rhodium(I). A New Descent of Series Approach to Alditols, Deoxyalditols, and Glycosylalditols

Unprotected Cn aldose sugars are cleanly decarbonylated by 1 equiv of chlorotris(triphenylphosphine)rhodium(I) in 1-24 h at 130 deg C in N-methyl-2-pyrrolidinone solution to give the corresponding Cn-1 alditol in about 75-95percent yields.This technique represents a useful variation on traditional carbohydrate “descent of series” reactions.The procedure is quite general and also works on a number of aldose derivatives, such as deoxy sugars, N-acetylated amino sugars, and disaccharides, providing convenient small-scale syntheses of deoxyalditols, (acetylamino)deoxyalditols, and glycosylalditols, respectively.The reactions proceed with complete retention of stereochemistry, the only side products observed being a few percent of the Cn lactones and the Cn-2 alditol.Attempts to make the reactions catalytic have not yet been very successful.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 14215-68-0 is helpful to your research., Application In Synthesis of N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide

Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics