Ontology highlight
ABSTRACT:
SUBMITTER: Buchy E
PROVIDER: S-EPMC4979966 | biostudies-literature | 2016
REPOSITORIES: biostudies-literature
Buchy Eric E Vukosavljevic Branko B Windbergs Maike M Sobot Dunja D Dejean Camille C Mura Simona S Couvreur Patrick P Desmaële Didier D
Beilstein journal of organic chemistry 20160606
The synthesis of ω-di-(trideuteromethyl)-trisnorsqualenic acid has been achieved from natural squalene. The synthesis features the use of a Shapiro reaction of acetone-d 6 trisylhydrazone as a key step to implement the terminal isopropylidene-d 6 moiety. The obtained squalenic acid-d 6 has been coupled to gemcitabine to provide the deuterated analogue of squalenoyl gemcitabine, a powerful anticancer agent endowed with self-assembling properties. The Raman spectra of both deuterated and non-deute ...[more]