Fairweather, Jon K.; Stick, Robert V.; Tilbrook, D. Matthew G. published the artcile< The asymmetric dihydroxylation of some alkenyl 2-acetylamino-2-deoxy-β-D-glucopyranosides: the preparation of optically pure epoxides as putative inhibitors of chitinases>, Product Details of C19H34O2, the main research area is aminodeoxyglucopyranoside epoxide preparation potential chitinase inhibitor; alkenyl aminodeoxyglucopyranoside asym hydroxylation.
Various alkenyl 2-acetylamino-2-deoxy-β-D-glucopyranosides have been subjected to the Sharpless asym. dihydroxylation protocol to yield the corresponding diols, albeit with somewhat disappointing stereoselectivity. An alternative, more traditional approach has yielded the optically pure epoxyalkyl 2-acetylamino-2-deoxy-β-D-glucopyranosides as putative inhibitors of chitinases. As well, an epoxypropyl chito-bioside and -trioside have been prepared, each as mixtures of two diastereoisomers.
Australian Journal of Chemistry published new progress about Dihydroxylation, stereoselective. 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Product Details of C19H34O2.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics