142389-71-7

Upstream product

• 142389-70-6 methyl 1-(but-3-yn-1-yl)cyclohexa-2,5-diene-1-carboxylate 
• 103669-19-8 methyl 1-(3-oxopropyl)cyclohexa-2,5-diene-1-carboxylate 
• 103669-18-7 methyl 1-(3-hydroxypropyl)cyclohexa-2,5-diene-1-carboxylate 
• 30889-20-4 methyl cyclohexa-2,5-diene-1-carboxylate 

Downstream Products

• 142389-72-8 tert-Butyl-(1-but-3-ynyl-cyclohexa-2,5-dienylmethoxy)-dimethyl-silane 
• 142389-73-9 5-[1-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-2,5-dienyl]-pent-2-yn-1-ol 
• 142389-74-0 (Z)-5-[1-(tert-Butyl-dimethyl-silanyloxymethyl)-cyclohexa-2,5-dienyl]-2-iodo-pent-2-en-1-ol 
• 142389-75-1 Acetic acid (Z)-5-[1-(tert-butyl-dimethyl-silanyloxymethyl)-cyclohexa-2,5-dienyl]-2-iodo-pent-2-enyl ester 
• 142410-10-4 3-[(Z)-5-(tert-Butyl-dimethyl-silanyloxy)-4-iodo-pent-3-enyl]-3-(tert-butyl-dimethyl-silanyloxymethyl)-cyclohexa-1,4-diene 

Relevant academic research and scientific papers

Synthesis of cycloalkanone-fused cyclopropanes by Au(I)-catalyzed oxidative ene-yne cyclizations

Au(I)-catalyzed oxidative cyclizations that successfully convert 1,5-ene-ynes and a 1,6-ene-yne to the corresponding cycloalkanone-fused cyclopropanes are described. This Au(I)-catalyzed oxidative cyclization can be effectively applied to various substrat

Further studies on a catalytic asymmetric synthesis of decalin derivatives

The decalin derivatives 2 (92% ee) and 18c (92% ee) were synthesized from the corresponding prochiral substrates 7b and 17a by an asymmetric Heck reaction.