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The lithiated derivative can react with electrophiles at either the - or - postions. It was found that conversion of the organolithium to an organotitanium reagent (by reaction with Ti(O-iPr)4), followed by reaction with e.g. cyclohexanecarboxaldehyde, resulted in regioselective reaction at the -position to give the corresonding hydroxy sulfide.
Ordering Information
Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Allyl ethyl sulfide, 1 g | sc-278682 | 1 g | $58.00 |