Hemi-thioacetal pummerer reaction for the synthesis of gliovirin benzylic sulfide models
The cyclic hemithioacetal sulfoxide 15 readily undergoes the Pummerer reaction in the presence of carbon nucleophiles to give substitute benzylic sulfides in excellent yields.
Magnus, Philip,Mitchell, Ian S.
p. 9131 - 9134
(2007/10/03)
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