141398-97-2

Upstream product

• 19550-89-1 2,2-dimethyl-5-hexen-3-ol 
• 141398-79-0 4,4-Dimethyl-1,1-bis(phenylseleno)-3-pentanol 
• 141398-76-7 4,4-Dimethyl-3-trimethylsilyloxypentanal 
• 141398-74-5 5,5-dimethyl-4-(trimethylsilyloxy)hex-1-ene 
• 645-96-5 Benzeneselenol 
• 141398-82-5 4,4-Dimethyl-1,1-bis(phenylseleno)-3-trimethylsilyloxypentane 
• 78-84-2 isobutyraldehyde 

Relevant academic research and scientific papers

Diastereomeric α-Phenylseleno Alkyllithium Compounds, Generation and Reactions

The selenoacetals 4 having a chiral center in the β-position were subjected to selenium/lithium exchange by butyllithium in ether.The resulting α-phenylseleno alkyllithium compounds 5 undergo rapid epimerization at -78 deg C.Trapping of these organolithiu