A highly enantiomeric excess in an asymmetric Pummerer-type rearrangement of chiral, non-racemic sulfoxides using O-silylated ketene acetal and the first successful Pummerer-type rearrangement on aromatic rings, are described.
No takes yet. Share an insight, caveat, or question.
Yasuyuki Kita (1997) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: