60814-34-8

Upstream product

• 60814-33-7 1-Ethynyl-2,6,6-trimethyl-2-cyclohexan-1-ol 
• 110890-64-7 3-ethynyl-2,4,4-trimethylcyclohex-2-en-1-one 
• 20013-73-4 2,6,6-trimethylcyclohex-2-en-1-one 
• 817203-17-1 2,4,4-trimethyl-3-(trimethylsilylethynyl)cyclohex-2-en-1-one 
• 817203-16-0 rac-2,6,6-trimethyl-1-(trimethylsilylethynyl)cyclohex-2-en-1-ol 

Downstream Products

• 85679-49-8 2,4,4-trimethyl-3-vinyl-cyclohex-2-enone 
• 875797-57-2 (+)-(R)-3-ethynyl-2,4,4-trimethylcyclohex-2-en-1-yl acetate 
• 875797-53-8 (-)-(S)-3-ethynyl-2,4,4-trimethylcyclohex-2-en-1-yl acetate 
• 1159988-03-0 (13S)-9-cis-4-oxo-13,14-dihydroretinoic acid 
• 1357598-66-3 ethyl (13S)-9-cis-4-oxo-13,14-dihydroretinoate 
• 1357598-64-1 ethyl (13S)-9-cis-4-hydroxy-13,14-dihydroretinoate 
• 1357598-75-4 ethyl (13R)-9-cis-4-hydroxy-13,14-dihydroretinoate 

Relevant academic research and scientific papers

A New Acetylene Rearrangement

Treatment of the enynols (1), (2), (3), and (5) with 35percent perchloric acid in tetrahydrofuran produces, through a series of prototropic shifts, the corresponding dienones (4) and (11).

Synthesis of ring-oxidized retinoids as substrates of mouse class I alcohol dehydrogenase (ADH1)

Ring-oxidized retinoids have been synthesized stereoselectively using the Stille cross-coupling reaction. Kinetic constants of mouse class I alcohol dehydrogenase (ADH1) with these retinoids were determined.