Hi,
I am trying to rearrange meso-hydrobenzoin ((1R,2S)-1,2-diphenylethane-1,2-diol ) to (1R,2R)-1,2-diphenylethane-1,2-diol (see pic for quick reference).
So basically just changing the chirality of one of the carbons, and keeping the other the same.
I've heard this can be done just with a strong base but I can't seem to find a paper on this anywhere - reaxys, WOS, google...
I've been looking at the Mitsunobu reaction, but I think that would spew out a mix of products as it would work on both alcohol groups?
Any ideas?
Thanks,
Mike