676591-53-0

Upstream product

• 1821-12-1 4-Phenylbutyric acid 
• 184370-68-1 1-((triisopropylsilyl)oxy)-4-pentyne 
• 177756-65-9 N-methoxy-N-methyl-4-phenylbutyramide 

Downstream Products

• 676591-56-3 (E)-(R)-8-Methoxy-2,2-dimethyl-11-phenyl-undec-6-enenitrile 
• 676591-55-2 (R)-1-phenyl-9-triisopropylsilanyloxynon-5-en-4-ol 
• 676591-60-9 (R)-triisopropyl-(6-methoxy-9-phenylnon-4-enyloxy)-silane 
• 676591-62-1 (R)-(9-iodo-4-methoxynon-5-enyl)benzene 
• 676591-61-0 (R)-6-methoxy-9-phenylnon-4-en-1-ol 
• 878168-56-0 (2S,4R,6S)-4-((E)-(R)-6-Methoxy-9-phenyl-non-4-enyl)-2-methyl-6-phenethyl-[1,3]dioxane-4-carbonitrile 
• 878168-57-1 (2R,4S,6R)-4-((E)-(R)-6-Methoxy-9-phenyl-non-4-enyl)-2-methyl-6-phenethyl-[1,3]dioxane-4-carbonitrile 
• 676591-54-1 (R)-1-phenyl-9-triisopropylsilanyloxynon-5-yn-4-ol 

Relevant academic research and scientific papers

Stereoselectivity of intramolecular SN′ cyclizations of alkyllithium reagents on methoxy alkenes

The cyclization of alkyllithium reagents onto methoxy alkenes has been investigated. The alkyllithium reagent was generated by reductive lithiation of an alkyl nitrile. In an unbiased substrate, a methoxy leaving group attached to a stereogenic secondary