The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.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, Application In Synthesis of (2R,3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl 2,2,2-trichloroacetimidate
C-ARYL-GLYCOSIDES AND 3-DEOXY-2-GLYCULOSONATES VIA INVERSE TYPE HETERO-DIELS-ALDER REACTION
The functionally substituted alpha,beta-unsaturated carbonyl compounds 1a,b provide with styrenes and with methyl alpha-methoxyacrylate in regiospecific and endo- and site-selective inverse type hetero-Diels-Alder reactions the dihydropyranes 2-4 and 9 respectively, which are readily transformed into C-aryl-beta-glycopyranosides and into methyl (methyl 3-deoxy-beta-arabino-2-heptulopyranosid)onates.Thus, from achiral precursors up to five new centers of chirality are generated in a three step procedure.
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 74808-09-6 is helpful to your research., Application In Synthesis of (2R,3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl 2,2,2-trichloroacetimidate
Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics