119146-01-9

Upstream product

• 60039-89-6 1,3-bis(phenylthio)cyclohexene 
• 90083-79-7 3-(Phenylthio)cyclohex-2-en-1-ol 
• 75717-39-4 3-(phenylsulfanyl)cyclohex-2-en-1-one 
• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 
• 22627-45-8 3-(3-butenyl)cyclohex-2-en-1-one 
• 119182-49-9 3-(3-oxobutan-1-yl)-1,3-bis(phenylthio)cyclohexene 

Relevant academic research and scientific papers

Asymmetric spirocyclization: A new type of acid-catalyzed intramolecular 1,4-addition to form carba-spirocyclic compounds

Novel spirocyclization based on intramolecular 1,4-addition and its asymmetric version have been developed using a combination of Lewis acid and 1,2-diol. Treatment of five- and six-membered α,β-unsaturated cyclic ketones having a 4-oxopentyl group at the

Usefully Functionalized Products from Conjugate Addition of Sulfur-Stabilized Anions to α-Enones

The addition to α,β-unsaturated ketones of a variety of organolithiums stabilized by at least two phenylthio groups provides mainly the 1,4-addition products at low temperatures in the absence of complexing agents such as HMPA.The products thus generated