199471-99-3

Upstream product

• 108-98-5 thiophenol 
• 199472-32-7 Acetic acid (4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-4-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl ester 
• 89956-14-9 [3-(2-Benzyloxyethyl)oxiran-2-yl]methanol 
• 199472-07-6 Methanesulfonic acid (1R,2S)-4-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-benzyloxy)-butyl ester 
• 199472-09-8 Acetic acid (1S,2S)-4-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-benzyloxy)-butyl ester 
• 199472-28-1 (2R,3S)-5-Benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentan-2-ol 
• 199472-30-5 Acetic acid (1S,2S)-1-(tert-butyl-diphenyl-silanyloxymethyl)-4-hydroxy-2-(4-methoxy-benzyloxy)-butyl ester 
• 199472-10-1 (3S,4S)-5-(tert-Butyl-diphenyl-silanyloxy)-3-(4-methoxy-benzyloxy)-pentane-1,4-diol 
• 199472-05-4 (2R,3S)-5-Benzyloxy-3-(4-methoxy-benzyloxy)-pentane-1,2-diol 
• 105-13-5 4-Methoxybenzyl alcohol 

Relevant academic research and scientific papers

The Synthesis of the Common C31-C40 Fragment of Pectenotoxins

The enantiomeric compound (2) corresponding to the common C31-C40 fragment of pectenotoxins, diarrhetic shellfish toxins, was first synthesized through the pathway involving the stereoselective generation of the α-lithiated tetrahydrofuran derivative (4) as the key stage.