126910-05-2

Upstream product

• 50-00-0 formaldehyd 
• 61950-54-7 (8aS)-1,1-(1,2-ethylenedioxy)-1,2,3,4,6,7,8,8a-octahydro-8a-methyl-6-oxonaphthalene 
• 108-98-5 thiophenol 
• 91444-85-8 (S)-8a'-methyl-5'-(phenylthiomethyl)-3',4',8',8a'-tetrahydro-2'H-spiro[[1,3]dioxolane-2,1'-naphthalen]-6'(7'H)-one 
• 882-33-7 diphenyldisulfane 

Relevant academic research and scientific papers

Regio- and stereoselective functionalizations of the Wieland-Miescher ketone derivatives at the C-8 position

New efficient methods for stereoselective hydroxymethylation, hydroxylation, and thiophenylation at the C-8 position of the Wieland-Miescher ketone derivatives (2-4) have been developed by diverse modifications from the Kirk-Petrow reaction, which involve autoxidation for the hydroxylation.Keywords - Wieland-Miescher ketone; Kirk-Petrow reaction; phenylthio-methylation; hydroxylation; hydroxymethylation; thiophenylation.