Abstract

The synthesis of the first homoleptic glucose derivative of a transition metal was achieved via the protonolysis of [V(C6H2Me3-2,4,6)3(thf)](thf = tetrahydrofuran) using the monoprotic ligand 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose (HL). The complex [VL3] was converted by addition of pyridine (py) into [VL3(py)2] containing a metal chiral centre as shown by X-ray analysis.

Full Text
Paper version not known

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 call

Disclaimer: 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.