1443230-63-4

Upstream product

• 1569102-73-3 (2S,4R,6S)-2-(4-methoxyphenylethyl)tetrahydro-6-(hydroxymethyl)-2H-pyran-4-ol 
• 56438-60-9 2-[2-(4-methoxyphenyl)ethyl]-1,3-dithiane 
• 1569102-86-8 (R)-1-(2-(4-methoxyphenylethyl)-1,3-dithian-2-yl)pent-4-en-2-ol 
• 20401-88-1 3-(4-methoxyphenyl)propional 
• 1569102-77-7 (3S,5R)-1-(4-methoxyphenyl)oct-7-ene-3,5-diol 
• 1569102-88-0 (R)-5-hydroxy-1-(4-methoxyphenyl)oct-7-en-3-one 
• 1569102-85-7 (S)-2-((2-(4-methoxyphenylethyl)-1,3-dithian-2-yl)methyl)oxirane 
• 5406-18-8 3-(p-methoxyphenyl)-1-propanol 
• 1569102-76-6 C₂₂H₂₇NO₄ 
• 1569102-74-4 ((2S,4R,6S)-6-(4-methoxyphenylethyl)tetrahydro-4-hydroxy-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate 
• 1443230-59-8 C₃₁H₃₈O₅S₂ 
• 1443230-67-8 C₄₀H₅₆O₃ 
• 1443230-65-6 C₂₈H₃₂O₃ 
• 1443230-66-7 C₃₀H₃₈O₉S₂ 

Downstream Products

• 1443256-45-8 (3S,5R)-1-(4-hydroxyphenyl)nonadecane-3,5-diol 

Relevant academic research and scientific papers

Stereoselective total synthesis of 4-((3S,5R)-3,5-dihydroxynonadecyl)phenol

A stereoselective total synthesis of 4-((3S,5R)-3,5-dihydroxynonadecyl) phenol has been accomplished in two different synthetic approaches. In the first approach, Prins cyclization has been successfully utilized to produce the anti-1,3-diol unit, which wa

Synthesis and configuration of the phenolic nonadecanediol isolated from the resinous exudates of heliotropium sinuatum

The (3S,5R) and (3R,5R) isomers of the title compound were synthesized from enantiopure epoxide chiral building blocks readily accessible from D-gluconolactone. The former (a syn-1,3-diol) gave 1H and 13C NMR spectroscopic data and optical rotation in good agreement with those reported for the natural product, whereas distinct differences were found with the data for the latter (an anti-1,3-diol). These results unambiguously showed that the absolute configuration of the natural product must be (3S,5R).