A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 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, COA of Formula: C8H15NO6
Regioselective Reductive Ring Opening of 4-Methoxybenzylidene Acetals of Hexopyranosides. Access to a Novel Protective Group Strategy
Reduction of fully protected 4,6-O-(4-methoxybenzylidene)hexopyranosides with sodium cyanoborohydride-trifluoroacetic acid in N,N-dimethylformamide, or with trimethylsilyl chloride in acetonitrile, gives the 6- and 4-O-(4-methoxybenzyl) ethers, respectively, in good yields and with good regioselectivity; the 4-methoxybenzyl ether linkage in products containing benzyl ethers or other protective groups is selectively cleaved upon treatment with cerium(IV) ammonium nitrate in aqueous acetonitrile.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.COA of Formula: C8H15NO6, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 14215-68-0, in my other articles.
Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics