172516-15-3

Upstream product

• 108-05-4 vinyl acetate 
• 122763-67-1 tert-butyl 3-hydroxypent-4-enoate 

Downstream Products

• 172516-19-7 (Z)-(5S,7S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-3-iodo-nona-2,8-dien-1-ol 
• 172516-18-6 (5R,7S)-5-(tert-Butyl-dimethyl-silanyloxy)-7-(tert-butyl-diphenyl-silanyloxy)-non-8-en-2-yn-1-ol 
• 172516-14-2 C₃₀H₄₄O₂Si₂ 
• 172516-16-4 (S)-3-(tert-Butyl-diphenyl-silanyloxy)-pent-4-enoic acid tert-butyl ester 
• 167892-85-5 (4R,6S)-6-(tert-Butyl-diphenyl-silanyloxy)-oct-7-en-1-yn-4-ol 
• 172516-17-5 (S)-3-((tert-butyldiphenylsilyl)oxy)pent-4-enal 
• 936703-26-3 (R)-3-((2S,3S)-3-(benzyloxy)-2-(tert-butoxycarbonylamino)-4-(cyclohexyloxy)-4-oxobutyloxy)-14-methylpentadecanoic acid 
• 936703-49-0 (2S,3S)-1-((R)-1-(allyloxy)-14-methyl-1-oxopentadecan-3-yl)-4-cyclohexyl-3-(benzyloxy)-2-(tert-butoxycarbonylamino)succinate 
• 949156-90-5 C₂₉H₅₂O₃Si₂ 
• 1040390-31-5 (3S)-3-hydroxy-4-pentenoic acid tert-butyl ester 

Relevant academic research and scientific papers

Studies toward the synthesis of pinnatoxins: The B,C,D-dispiroketal fragment

A stereoselective synthesis of the tricyclic B,C,D-dispiroketal fragment of pinnatoxins is described. Both products of an efficient enzymatic resolution reaction are used to set the stereochemistry of C12 and C23, which have opposite configuration. The co

Fluorogenic stereochemical probes for transaldolases

Transaldolase catalyzes the transfer of dihydroxyacetone from, for example, fructose 6-phosphate to erythrose 4-phosphate. As a potential probe for assaying fluorescent transaldolase, 6-O-coumarinyl-fructose (1) was prepared in six steps from D-fructose.