454181-34-1

Upstream product

• 454181-39-6 C₄₄H₅₆O₂Si₂ 
• 454181-44-3 C₃₉H₄₆O₂Si₂ 
• 454181-46-5 (E)-(S)-4-(tert-Butyl-diphenyl-silanyloxy)-dodec-2-en-6-yn-1-ol 
• 454181-41-0 (E)-(S)-4-(tert-Butyl-diphenyl-silanyloxy)-dodec-2-en-6-ynal 
• 454181-36-3 (E)-(S)-7-(tert-Butyl-diphenyl-silanyloxy)-hept-5-en-1-yn-4-ol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 110-53-2 1-Bromopentane 
• 454181-35-2 [(S)-((E)-1-But-1-en-3-ynyl)-non-3-ynyloxy]-tert-butyl-diphenyl-silane 
• 41349-38-6 methyl 7-bromohept-5-ynoate 

Downstream Products

• 100428-43-1 methyl 12(S)-<(tert-butyldiphenylsilyl)oxy>-5(Z),8(Z),10(E),14(Z)-eicosatetraenoate 

Relevant academic research and scientific papers

A versatile asymmetric synthesis of highly enantiomerically enriched 12(S)-HETE via a combination of enzymatic and chemical processes

This paper describes a versatile asymmetric synthesis of highly enantiomerically enriched 12(S)-HETE via enzymatic kinetic resolution of the key allylic alcohol synthon and the facile introduction of three alkyne units which were concomitantly converted t