Application of 129-64-6, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 129-64-6, Name is (3aR,4S,7R,7aS)-rel-3a,4,7,7a-Tetrahydro-4,7-methanoisobenzofuran-1,3-dione, SMILES is O=C1OC([C@]2([H])[C@](C3)([H])C=C[C@]3([H])[C@@]21[H])=O, belongs to benzoxazole compound. In a article, author is Wu, Yu-Ran, introduce new discover of the category.
Synthesis and anticholinesterase activities of novel glycosyl benzoxazole derivatives
Eight glycosyl benzoxazole derivatives are synthesized by nucleophilic addition reactions of glycosyl isothiocyanate witho-aminophenol in tetrahydrofuran. The reaction conditions are optimized, and good yields (86%-94%) were obtained. The structures of all new products are confirmed by infrared,H-1 nuclear magnetic resonance, and high-resolution mass spectrometry (electrospray ionization). In addition, the in vitro cholinesterase inhibitory activities of these new compounds are tested by Ellman’s method.
Application of 129-64-6, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 129-64-6.
Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem