408358-01-0

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 55058-51-0 (4S)-hydroxy-(6R)-2,2,6-trimethylcyclohexanone 

Downstream Products

• 26666-93-3 meso-alloxanthin 
• 408358-15-6 3-[(4S)-4-tert-butyldimethylsilyloxy-2,6,6-trimethylcyclohex-1-enyl]propyl acetate 
• 408358-14-5 3-[(4S)-4-tert-butyldimethylsilyloxy-2,6,6-trimethylcyclohex-1-enyl]propan-1-ol 
• 408358-13-4 2-[(4S)-4-tert-butyldimethylsilyloxy-2,6,6-trimethylcyclohex-1-enyl]ethanol 
• 409088-76-2 3-[(4S)-4-tert-butyldimethylsilyloxy-2,6,6-trimethylcyclohex-1-enyl]propanenitrile 
• 408358-03-2 (4S,6R)-4-tert-butyldimethylsilyloxy-1-ethynyl-2,2,6-trimethylcyclohexanol 
• 408358-04-3 [(4S)-4-tert-butyldimethylsilyloxy-2,6,6-trimethylcyclohex-1-enyl]acetaldehyde 
• 408358-02-1 (4S,6R)-1-Ethynyl-2,2,6-trimethyl-cyclohexane-1,4-diol 

Relevant academic research and scientific papers

Synthesis of (3S,3′S)- and meso-stereoisomers of alloxanthin and determination of absolute configuration of alloxanthin isolated from aquatic animals

In order to determine the absolute configuration of naturally occurring alloxanthin, a HPLC analytical method for three stereoisomers 1a-c was established by using a chiral column. Two authentic samples, (3S,3?S)- and meso-stereoisomers 1b and 1c, were ch

Carotenoids and related polyenes. Part 7. Total synthesis of crassostreaxanthin B applying the stereoselective rearrangement of tetrasubstituted epoxides

(3R,3′S)- and (3R,3′R)-Crassostreaxanthin B isomers are synthesized by application of the stereoselective rearrangement of tetrasubstituted epoxides 5a,b. As a result, the absolute configuration at C-3′ of 1 is determined to be S.