593254-85-4

Upstream product

• 108-24-7 acetic anhydride 
• 521309-79-5 methyl (2R,3R)-3-hydroxy-2-tetracosanyl-13-(t-butyldiphenylsilyloxy)tridecanoate 
• 116137-78-1 C₁₄H₂₇BrMgO₂ 
• 566896-88-6 (R)-(+)-1-benzyloxy-3-(tert-butyldimethylsilyloxy)-13-(tetrahydropyran-2-yloxy)tridecane 
• 593254-82-1 methyl (R)-3-hydroxy-13-(t-butyldiphenylsilyloxy)tridecanoate 
• 873567-31-8 (R)-1-hydroxy-3-(tert-butyldimethylsilyloxy)-13-(tetrahydropyran-2-yloxy)tridecane 
• 521309-77-3 (R)-(+)-1-benzyloxy-3-hydroxy-13-(tetrahydropyran-2-yloxy)tridecane 
• 521309-78-4 methyl (R)-3,13-dihydroxytridecanoate 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 143-15-7 1-dodecylbromide 
• 6946-24-3 1-tetracosyl bromide 
• 506-51-4 tetracosyl alcohol 
• 62127-55-3 1-iodotetracosane 
• 3344-77-2 12-bromododecanol 

Downstream Products

• 521309-82-0 (R)-2-((R)-1-acetoxy-12-{(1S,2R)-2-[14-((1S,2R)-2-eicosylcyclopropyl)tetradecyl]cyclopropyl}dodec-11-enyl)hexacosanoic acid methyl ester 

Relevant academic research and scientific papers

The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis

We report a synthesis of a single enantiomer of a mycolic acid from Mycobacterium tuberculosis containing a di-cis-cyclopropane. The method can be simply varied to modify the chain lengths or the absolute stereochemistry of either cyclopropane.

The synthesis of a single enantiomer of a major α-mycolic acid of Mycobacterium tuberculosis

We report a synthesis of a single enantiomer of a dicyclopropane containing mycolic acid from Mycobacterium tuberculosis; this method can be simply varied to modify the chain lengths or the absolute stereochemistry of either cyclopropane.