670223-09-3

Upstream product

• 670223-05-9 (S)-2-cyclohexylsulfanyl-N,N-dimethylpent-4-enamide 
• 670223-06-0 (SS,2S)-2-cyclohexylsulfinyl-N,N-dimethylpent-4-enamide 
• 385837-48-9 (SS,2S)-2-cyclohexylsulfinyl-N,N-dimethylpent-4-enethioamide 
• 226709-30-4 (R)-2-(Cyclohexylsulfinyl)-N,N-dimethylethanethioamide 

Downstream Products

• 890706-53-3 methyl (4R)-2-cyclohexylsulfanyl-3-oxiranylpropanoate 
• 890706-52-2 (5S)-3-cyclohexylsulfanyl-5-methyl-5H-furan-2-one 
• 890706-54-4 (5S)-3-cyclohexylsulfanyl-5-ethyl-dihydrofuran-2-one 
• 890706-57-7 (5S)-3-cyclohexylsulfanyl-5-ethyl-5-H-furan-2-one 
• 890706-58-8 (5S)-3-cyclohexanesulfinyl-5-ethyl-5-H-furan-2-one 

Relevant academic research and scientific papers

Studies directed towards the enantioselective synthesis of ethisolide and isoavenaciolide

An asymmetric synthesis of an analog of ethisolide has been achieved by using as key steps two σ[3,3]rearrangements stereocontrolled by a sulfinyl group. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Asymmetric Induction of the Iodolactonization Reaction of α-Sulfurated γ-Unsaturated Amides

The 1,3-asymmetric iodolactonization reaction of enantiopure α-sulfurated γ-unsaturated amides has been investigated. With sulfinyl and sulfonyl groups, a poorly stereoselective reaction was observed, whereas with a sulfanyl moiety, the diastereoselectivi