In heterogeneous catalysis, catalysts provide a surface to which reactants bind in a process of adsorption. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction. 74808-09-6, Name is (2R,3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl 2,2,2-trichloroacetimidate, molecular formula is C36H36Cl3NO6. In a Article，once mentioned of 74808-09-6, Safety of (2R,3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl 2,2,2-trichloroacetimidate
Glycopyranosyl trichloroacetimidates react with SmI2/O2/THF to give 4- iodo-n-butyl 1,2-transglycopyranosides. Good to high yields can be obtained from 2alpha-O-acylated trichloroacetimidates. With armed or manno substrates competitive formation of alpha-glycopyranosyl iodides occurs.
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Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics