124629-72-7

Upstream product

• 97579-27-6 C₃₇H₄₆O₆ 
• 118789-49-4 C₃₄H₄₂O₆ 
• 1053634-06-2 (R)-1-[(4R,5R)-5-((R)-1-Hydroxy-non-3-ynyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-non-3-yn-1-ol 
• 42017-07-2 1-heptynyllithium 
• 75-47-8 iodoform 
• 124629-64-7 4(R)-benzoyloxy dodec-2(E)-en-6-ynal 
• 124629-63-6 2(R)-benzoyloxy-dec-4-ynal 
• 98-88-4 benzoyl chloride 
• 74-88-4 methyl iodide 

Downstream Products

• 131937-96-7 ester methylique du 12-O-benzoyl-LTB₄ 
• 83058-42-8 Methyl (5S,6Z,8E,10E,12R,14Z)-5,12-Dihydroxyeicosa-6,8,10,14-tetraenoate 
• 124629-71-6 12(R)-benzoyloxy-5(S)-hydroxy icosa-8(E),10(E)-diene 6,14-diynoate de methyle 
• 124629-71-6 Benzoic acid (2E,4Z)-(1R,8R)-8-hydroxy-11-methoxycarbonyl-1-oct-2-ynyl-undeca-2,4-dien-6-ynyl ester 
• 124629-73-8 12(R)-benzoyloxy-5(S)-hydroxy icosa-8(Z),10(E)-diene 6,14-diynoate de methyle 

Relevant academic research and scientific papers

Synthesis of 12-O-benzoyl 6,7,14,15-tetrahydro leucotriene B4 methyl ester, a precursor of labelled LTB4.

Leucotriene B4 (LTB4), a 5-lipoxygenase metabolite of arachidonic acid, is an important mediator of inflammatory processes and of acute hypersensitivity reactions.The availability of isotopically labelled versions of this natural metabolite is of primary

Total synthesis of 12-O-benzoyl-6,7,14,15-tetradehydro leukotriene B4 methyl ester: precursor of labeled LTB4

12-O-Benzoyl-6,7,14,15-tetrahydroleukotriene B4 methyl ester 1, the direct precursor of isotopically labeled LTB4's, has been prepared.This synthesis was accomplished by the assembly of two key chirons: α-hydroxyaldehyde of R confiur