1376185-96-4

Upstream product

• 1376185-66-8 (2E)-3-methyl-5-[(4R)-2,6,6-trimethyl-4-triethylsilyloxycyclo-hex-1-en-1-yl]pent-2-en-4-yn-1-1ol 
• 1376185-70-4 [(1R)-4-((3E)-5-chloro-3-methylpent-3-en-1-ynyl)-3,5,5-trimethylcyclohex-3-en-1-yloxy]triethylsilane 
• 5056-17-7 2,7-dimethyl-2,4,6-octanetriene-1,8-dialdehyde 
• 1376185-61-3 triethyl[(4R)-4-ethynyl-3,5,5-trimethylcyclohex-3-en-1-yl]-oxysilane 
• 20548-02-1 (4R,6R)-4-hydroxy-2,2,6-trimethylcyclohexan-1-one 
• 118829-40-6 (R)-4-ethynyl-3,5,5-trimethylcyclohex-3-en-1-ol 
• 83646-59-7 1(S),4(R),6(R)-1-ethynyl-2,2,6-trimethyl-1,4-cyclohexanediol 
• 76530-42-2 (R)-4-ethynyl-3,5,5-trimethylcyclohex-3-enyl acetate 
• 152125-31-0 (4R,6R)-2,2,6-Trimethyl-4-trimethylsilanyloxy-cyclohexanone 
• 994-30-9 triethylsilyl chloride 

Downstream Products

• 26666-93-3 (3R',3'R)-alloxanthin 

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

Stereoselective total synthesis of the acetylenic carotenoids alloxanthin and triophaxanthin

Stereoselective total synthesis of the C40-diacetylenic carotenoid alloxanthin (1) and the C31-acetylenic apocarotenoid triophaxanthin (2) was accomplished by Wittig condensation of C 10-dialdehyde 20 or C16-ket