1027062-81-2

Upstream product

• 83646-59-7 1(S),4(R),6(R)-1-ethynyl-2,2,6-trimethyl-1,4-cyclohexanediol 
• 70905-65-6 1(R),4(S),5(R)-4-ethynyl-4-hydroxy-3,3,5-trimethyl-cyclohexyl acetate 
• 152125-31-0 (4R,6R)-2,2,6-Trimethyl-4-trimethylsilanyloxy-cyclohexanone 
• 214335-59-8 Acetic acid (1R,5R)-3,3,5-trimethyl-4-[2-oxo-eth-(Z)-ylidene]-cyclohexyl ester 
• 214335-60-1 Acetic acid (R)-4-(2-hydroxy-ethyl)-3,5,5-trimethyl-cyclohex-3-enyl ester 
• 69297-04-7 Acetic acid (R)-3,5,5-trimethyl-4-(2-oxo-ethyl)-cyclohex-3-enyl ester 
• 180039-17-2 Acetic acid (R)-4-(2-methanesulfonyloxy-ethyl)-3,5,5-trimethyl-cyclohex-3-enyl ester 

Downstream Products

• 180039-18-3 (1R)-4-ethyl-3,5,5-trimethylcyclohex-3-enyl acetate 

Relevant academic research and scientific papers

Carotenoids and related polyenes. Part 5. Lewis acid-promoted stereoselective rearrangement of 5,6-epoxy carotenoid model compounds

The novel acyclic tetrasubstituted olefinic end group and the cyclopentyl end group of carotenoids were obtained by Lewis acid-promoted stereoselective rearrangement of the epoxide end group of 5,6-epoxy carotenoids. The scope and limitation of this rearr

Stereoselective rearrangement of 5,6-epoxy carotenoid model compounds

Carotenoids with novel acyclic tetrasubstituted olefinic and cyclopentyl end groups are obtained by Lewis acid-promoted stereoselective rearrangement of the epoxide end group of 5,6-epoxy carotenoids.