Abstract
The hydroxy groups of D-mannitol were protected by the formation of acetals and benzylethers and then 2-O-benzyl-D-glyceraldehyde dimethylacetal was prepared after the deprotection and oxygenolysis of the protected D-mannitol. In the presence of DCC and DMAP, the lauroyl group was introduced at the primary hydroxyl group of the dimethylacetal and 3-O-lauroyl-2-O-benzyl-glycerol was obtained after the deprotection of the dimethylacetal with FeCl3·6H2O and then reduction with NaBH4. A series of new 3-O-lauroyl-2-O-benzyl-glycerol sulfonates was synthesised by the coupling of different sulfonyl groups with the 3-O-lauroyl-2-O-benzyl- glycerol. The bioactivities of the title compounds were tested and some compounds exhibited fungicidal activity against the tested fungi.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
