1-(Trimethylsilyloxy)cyclohexene
98.0%(GC)
science Other reagents with same CAS 6651-36-1
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description Product Description
Used as a silyl enol ether in organic synthesis, particularly in Mukaiyama aldol reactions where it acts as a nucleophilic enolate equivalent. It is valuable for forming carbon-carbon bonds under mild, Lewis acid-catalyzed conditions. Commonly employed in the synthesis of complex molecules such as natural products and pharmaceuticals due to its stability and reactivity profile. Also serves as a protecting group reagent for enolizable carbonyl compounds during multistep syntheses.
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