449753-95-1

Upstream product

• 98-88-4 benzoyl chloride 
• 7383-19-9 hept-1-yn-3-ol 
• 75045-85-1 (+/-)-1-(trimethylsilyl)hept-1-yn-3-ol 
• 110-62-3 pentanal 

Downstream Products

• 449753-99-5 methyl rac-16-benzoyloxy-5,8,11,14-eicosatetraynoate 
• 449754-00-1 methyl rac-(5Z,8Z,11Z,14Z)-16-benzoyloxy-5,8,11,14-eicosatetraenoate 
• 128914-46-5 (16S,5Z,8Z,11Z,14Z)-16-hydroxy-5,8,11,14-eicosatetraenoic acid 
• 128914-46-5 (16R,5Z,8Z,11Z,14Z)-16-hydroxy-5,8,11,14-eicosatetraenoic acid 
• 449753-98-4 rac-5-(benzoyloxy)-14-bromotetradeca-6,9,12-triyne 
• 449753-97-3 rac-10-(benzoyloxy)tetradeca-2,5,8-triyn-1-ol 
• 51703-66-3 (S)-(-)-1-heptyn-3-ol 
• 51703-65-2 (R)-1-heptyn-3-ol 

Relevant academic research and scientific papers

A simple method for the preparation of (5Z,8Z,11Z,14Z)-16-Hydroxyeicosa-5,8,11,14-tetraenoic acid enantiomers and the corresponding 14,15-Dehydro analogues: Role of the 16-Hydroxy group for the lipoxygenase reaction

(5Z,8Z,11Z,13E)-15-Hydroxy-5,8,11,13-eicosatetraenoic acid (15-HETE) is not well oxygenated by arachidonate 15-lipoxygenases because of two structural reasons: (i) it contains a hydrophilic OH-group in close proximity to its methyl end and (ii) it lacks t

The effect of catechin derivatives on the enantioselectivity of lipase-catalyzed hydrolyses of alkynol benzoate esters

Polyphenols, such as (+)-catechin and pyrogallol could be used to enhance stereochemical control in the lipase-catalyzed hydrolysis of alkynol benzoate esters, leading to increased enantioselectivities in the kinetic resolution of alkynols with lipase Amano AH.