592508-24-2

Upstream product

• 592508-21-9 tert-Butyl-[(E)-(S)-4-(4-methoxy-phenoxy)-1-methyl-but-2-enyloxy]-diphenyl-silane 
• 592508-22-0 (E)-(S)-5-(4-Methoxy-phenoxy)-pent-3-en-2-ol 
• 203387-35-3 (E)-(S)-4-(tert-butyl-diphenyl-silanyloxy)-pent-2-enoic acid ethyl ester 
• 189630-90-8 (4S,2E)-4-[(tert-butyldiphenylsilyl)oxy]pent-2-en-1-ol 
• 592508-23-1 (3S,4E)-3-(4-methoxy-phenoxymethyl)-hex-4-enoic acid dimethylamide 

Downstream Products

• 592508-25-3 (E)-(S)-5-(4-Methoxy-phenoxymethyl)-octa-1,6-dien-3-ol 

Relevant academic research and scientific papers

Enantioselective synthesis of the carbocyclic moiety of (-)-carbovir

Enantioselective construction of the protected carbocycle moiety of the anti-HIV drug carbovir was achieved in 11 steps from (S)-(-)-ethyl lactate. The two key steps are a Claisen [3+3] sigmatropic rearrangement of (3S,4E)-3-(4-methoxy-phenoxymethyl)-hex-