1373398-07-2

Upstream product

• 108-98-5 thiophenol 
• 79597-59-4 3-Methyl-4-phenylthio-2-butensaeure-ethylester 
• 5042-53-5 1-(phenylsulfanyl)acetone 
• 1373398-04-9 C₁₁H₁₄OS 
• 1373398-06-1 C₁₅H₁₈O₂S 

Downstream Products

• 1373398-09-4 C₁₈H₂₄O₃S 
• 1373398-08-3 C₁₇H₂₂O₃S 
• 1542793-82-7 C₂₃H₃₈O₄SSi 
• 1542794-53-5 C₂₃H₃₈O₂SSi 
• 1542794-50-2 C₁₇H₂₄O₂S 
• 1542794-49-9 C₁₇H₂₂O₂S 

Relevant academic research and scientific papers

Stereoselective synthesis of the C3-C12 subunit of laulimalide

A stereoselective synthesis of the C3-C12 subunit of the tumor growth inhibitors laulimalide is disclosed. The key steps of the synthesis include asymmetric alkylation using Oppolzer's protocol and an asymmetric hetero-Diels-Alder reaction using Jacobsen'

Stereoselective synthesis of the C3-C12 subunit of laulimalide

A stereoselective synthesis of the C3-C12 subunit of the tumor growth inhibitors laulimalide is disclosed. The key steps of the synthesis include asymmetric alkylation using Oppolzer's protocol and an asymmetric hetero-Diels-Alder reaction using Jacobsen'

Stereoselective synthesis of the macrolactone core of (+)-neopeltolide

A stereoselective synthesis of the macrolactone core of the potent anticancer agent neopeltolide is disclosed. The key steps of the synthesis include asymmetric allylation using Krische' protocol, conjugate reduction using MacMillan's methodology, and an