16326-89-9

Upstream product

• 22412-89-1 cycloocta-2,4,6-trien-1-one 
• 1067-71-6 Diethyl (2-oxopropyl)phosphonate 
• 80466-34-8 2,4-hexadienal 
• 16326-87-7 1-methyl-cycloocta-2c,4c,6c-trienol 

Downstream Products

• 73901-91-4 1-(2-(1,3-pentadienyl)-4-tert-butyldimethylsilyloxycyclohex-3-enyl)-3-phenylpropyn-1-one 
• 73901-99-2 1,2,4a,4b,7,9a-hexahydro-7-methyl-8-phenyl-3-tert-butyldimethylsilyloxy-9H-fluoren-9-one 
• 73901-98-1 1,2,4a,4b,7,8,8a,9a-octahydro-7-methyl-8-phenyl-3-tert-butyldimethylsilyloxy-9H-fluoren-9-one 
• 73901-92-5 1-(2-(1,3-pentadienyl)-1-methyl-4-tert-butyldimethylsilyloxycyclohex-3-enyl)-3-phenylpropyn-1-one 
• 73902-00-8 1,2,4a,4b,7,9a-hexahydro-7,9a-dimethyl-8-phenyl-3-tert-butyldimethylsilyloxy-9H-fluorene-9-one 

Relevant academic research and scientific papers

Addition en 1,8 d'organocuprates lithiens satures sur la cetone CH3(CH=CH)3COCH3 et sur l'ester CH3(CH=CH)3COOC2H5

The reaction of saturated lithium organocuprates with the trienic ketone CH3(CH=CH)3COCH3 and with the trienic ester CH3(CH=CH)3COOC2H5 proceeds by a 1,8 conjugate addition to give a β,δ-diethylenic carbonyl compound.