160017-32-3

Upstream product

• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 160017-28-7 (5Z,8Z)-(S)-10-[(4R,5R)-2,2-Dimethyl-5-((Z)-oct-2-enyl)-[1,3]dioxolan-4-yl]-10-(4-methoxy-benzyloxy)-deca-5,8-dienoic acid methyl ester 
• 160080-76-2 (3aR,7S,7aS)-7-Hydroxy-2,2-dimethyl-3a,4,7,7a-tetrahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester 
• 16666-79-8 hexylidenetriphenylphosphoran 
• 160017-29-8 (5Z,8Z,14Z)-(10S,11R,12R)-11,12-Dihydroxy-10-(4-methoxy-benzyloxy)-icosa-5,8,14-trienoic acid methyl ester 
• 160017-25-4 (3aR,7S,7aR)-7-(4-Methoxy-benzyloxy)-2,2-dimethyl-3a,4,7,7a-tetrahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester 
• 160017-27-6 (S)-2-[(4R,5R)-2,2-Dimethyl-5-((Z)-oct-2-enyl)-[1,3]dioxolan-4-yl]-2-(4-methoxy-benzyloxy)-ethanol 

Downstream Products

• 160017-33-4 Benzoic acid (2Z,5Z)-(R)-9-methoxycarbonyl-1-[(2R,3S)-((Z)-3-oct-2-enyl)-oxiranyl]-nona-2,5-dienyl ester 
• 94161-10-1 10(S),11(S),12(S)-hepoxilin B₃ 
• 94161-10-1 10(R),11(S),12(S)-hepoxilin B₃ 

Relevant academic research and scientific papers

Hepoxilins B3: Synthesis of all four stereoisomers and a glutathione adduct

Utilizing (-)-quinic acid as a differentiated bis-aldehyde chiron, both pairs of hepoxilin B3 enantiomers and a glutathione adduct were synthesized by regiospecific functionalization of an acyclic vic-diol.