670223-06-0

Upstream product

• 385837-48-9 (SS,2S)-2-cyclohexylsulfinyl-N,N-dimethylpent-4-enethioamide 
• 226709-30-4 (R)-2-(Cyclohexylsulfinyl)-N,N-dimethylethanethioamide 
• 106-95-6 allyl bromide 

Downstream Products

• 670223-09-3 (3S,5R)-4,5-dihydro-3-cyclohexylsulfanyl-5-iodomethyl-2(3H)-furanone 
• 890706-49-7 3-cyclohexanesulfinyl-5-iodomethyl-3-phenylselanyl-dihydro-furan-2-one 
• 890706-46-4 3-cyclohexanesulfinyl-5-methyl-3-phenylselanyl-dihydro-furan-2-one 
• 890706-58-8 (5S)-3-cyclohexanesulfinyl-5-ethyl-5-H-furan-2-one 
• 890706-53-3 methyl (4R)-2-cyclohexylsulfanyl-3-oxiranylpropanoate 
• 890706-57-7 (5S)-3-cyclohexylsulfanyl-5-ethyl-5-H-furan-2-one 
• 890706-54-4 (5S)-3-cyclohexylsulfanyl-5-ethyl-dihydrofuran-2-one 
• 890706-52-2 (5S)-3-cyclohexylsulfanyl-5-methyl-5H-furan-2-one 
• 890706-45-3 3-cyclohexanesulfinyl-5-methyl-dihydro-furan-2-one 

Relevant academic research and scientific papers

Highly stereoselective C-allylation of an enantiopure α-sulfinyl thioacetamide

The alkylation of the lithium enolate of enantiopure α-cyclohexylsulfinyl thioacetamide 1 with allyl bromides 5 possessing an electron-withdrawing group at the vinylic position does not occur at the sulfur center - as expected in the sulfur series - but a

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