144880-26-2

Upstream product

• 502-44-3 hexahydro-2H-oxepin-2-one 
• 137305-47-6 5-methyl-8-(trimethylsilyl)oct-7-yne-1,6-diol 
• 144880-22-8 5-Methyl-6-oxo-oct-7-ynal 
• 137305-48-7 5-methyloct-7-yne-1,6-diol 
• 144880-16-0 6-hydroxy-2-methylhexanal 
• 2549-61-3 3-methylcaprolactone 
• 144880-24-0 (E)-8-(4-Methoxy-phenylsulfanyl)-5-methyl-6-oxo-oct-7-enal 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 144880-32-0 methyl (+/-)-(3aR*,4S*,5S*,7aS*)-7-(tert-butyldimethylsiloxy)-3a,4,5,7a-tetrahydro-5-(4-methoxyphenylthio)-7a-methylindane-4-carboxylate 
• 144880-32-0 methyl (+/-)-(3aR*,4S*,5R*,7aR*)-7-(tert-butyldimethylsiloxy)-3a,4,5,7a-tetrahydro-5-(4-methoxyphenylthio)-7a-methylindane-4-carboxylate 
• 144880-36-4 methyl (+/-)-(3aR*,4S*,5S*,7aS*)-3a,4,5,6,7,7a-hexahydro-5-(4-methoxyphenylthio)-7a-methyl-7-oxoindane-4-carboxylate 
• 144880-36-4 methyl (+/-)-(3aR*,4S*,5R*,7aR*)-3a,4,5,6,7,7a-hexahydro-5-(4-methoxyphenylthio)-7a-methyl-7-oxoindane-4-carboxylate 

Relevant academic research and scientific papers

Sulfur-mediated Intramolecular Double Michael-Type Reaction: Synthesis of trans-Hydroindanes and Mechanism

A sulfur-mediated intramolecular double Michael-type reaction stereoselectively producing trans-hydroindanes was developed. ε-Caprolactone 3 was transformed into four isomers of methyl 7-methyl-8-oxo-10-(phenylthio)deca-2,9