97579-36-7

Upstream product

• 4762-26-9 hexyltriphenylphosphonium bromide 
• 107996-41-8 (Z)-(R)-1-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-non-3-en-1-ol 
• 113725-68-1 (1R,2R)-1-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-1-(2-ethoxy-ethoxy)-dec-4-yn-2-ol 
• 42017-07-2 1-heptynyllithium 
• 97579-33-4 C₃₄H₄₆O₆ 
• 111037-24-2 Benzoic acid (Z)-(R)-1-((R)-1,2-dihydroxy-ethyl)-non-3-enyl ester 
• 16666-79-8 hexylidenetriphenylphosphoran 
• 97579-27-6 C₃₇H₄₆O₆ 
• 97579-31-2 C₃₇H₅₀O₆ 
• 136298-20-9 2-deoxy-4,5-O-isopropylidene-3-O-benzoyl-D-threo-pentose diethyl dithioacetal 
• 136298-22-1 Benzoic acid (R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-oxo-propyl ester 
• 98-88-4 benzoyl chloride 
• 111037-23-1 2(R),3(R) 1,2-O-isopropylidene-3-O-benzoyl-5Z-undecene 
• 60106-53-8 n-hexyltriphenylphosphonium iodide 

Downstream Products

• 128855-31-2 (3Z,5R,7Z)-5-Benzoyloxytrideca-3,7-dien-1-yne 
• 128855-30-1 (3E,5R,7Z)-5-Benzoyloxytrideca-3,7-dien-1-yne 
• 136298-21-0 10(R)-methyl-10-O-benzoyl-8E,12Z-octadecadienoate 
• 83058-42-8 Methyl (5S,6Z,8E,10E,12R,14Z)-5,12-Dihydroxyeicosa-6,8,10,14-tetraenoate 
• 71160-24-2 Leukotriene B 
• 111037-26-4 (3R,5Z)-3-(Benzoyloxy)-1-bromoundeca-1,5-diene 

Relevant academic research and scientific papers

Total synthesis of (+)-leukotriene B4 methyl ester and its 5-epimer from (R)-glycidol

The Pd-Cu coupling reaction of a chiral hydroxy-(E,E)-iododiene with a racemic acetylenic alcohol followed by reduction of the dienyne leads to the desired (Z,E,E) geometry and allows synthesis of LTB4 and its 5-epimer after separation of diast

Stereoselective total synthesis of 10-(R)-hydroxy-8E,12Z-octadecadienoic acid: The fungitoxic compound in timothy plant

A convenient synthesis of 10-(R)-hydroxy-8E,12Z-ocatadecadienoic acid, the fungitoxic compound in the timothy plant (Phleum pratense) against leaf spot disease is described utilising D-xylose as chiral source.

OPTICALLY ACTIVE PROPARGYLIC ALCOHOLS FROM D-XYLOSE USEFUL PRECURSORS FOR LTB4 SYNTHESIS

Using D-Xylose as a source of chirality at C-5 and C-12 in LTB4, an efficient synthesis of the optically active propargylic alcohols A and B, chiral precursors for the LTB4 synthesis, has been achieved.

A Practical Preparation of α-Hydroxy and α,β-Dihydroxy Aldehydes, Useful Intermediates for the Synthesis of Arachidonic Acid Metabolites, starting with D-Glyceraldehyde Acetonide

Optically active α-hydroxy and α,β-dihydroxy aldehydes, useful intermediates for synthesis of lipoxygenase metabolites of arachidonic acid, are synthesized highly diastereoselectively starting with readily available D-glyceraldehyde acetonide.