115944-89-3

Upstream product

• 115920-15-5 Benzoic acid (1S,2S,6R,7S,8R,9R)-6,8-diacetoxy-10,12-dioxa-tricyclo[7.2.1.0^2,7]dodec-4-en-4-ylmethyl ester 
• 115944-87-1 Benzoic acid (1S,3R,4R,4aS,5R,8aS)-3,4,5-triacetoxy-1-acetoxymethyl-3,4,4a,5,8,8a-hexahydro-1H-isochromen-7-ylmethyl ester 
• 115920-19-9 Benzoic acid (1S,4R,4aS,5R,8R,8aR)-4,5,8-triacetoxy-1-acetoxymethyl-3-oxo-3,4,4a,5,8,8a-hexahydro-1H-isochromen-7-ylmethyl ester 
• 115920-17-7 Benzoic acid (1S,4R,4aR,5R,8S,8aR)-5-acetoxy-1-acetoxymethyl-4,8-dihydroxy-3-oxo-3,4,4a,5,8,8a-hexahydro-1H-isochromen-7-ylmethyl ester 
• 115920-17-7 Benzoic acid (1S,4R,4aR,5R,8R,8aR)-5-acetoxy-1-acetoxymethyl-4,8-dihydroxy-3-oxo-3,4,4a,5,8,8a-hexahydro-1H-isochromen-7-ylmethyl ester 
• 115920-18-8 Benzoic acid (1S,4R,4aR,5R,8aS)-5-acetoxy-1-acetoxymethyl-4-hydroxy-3,8-dioxo-3,4,4a,5,8,8a-hexahydro-1H-isochromen-7-ylmethyl ester 
• 115920-16-6 Benzoic acid (1S,4R,4aR,5R,8aS)-5-acetoxy-1-acetoxymethyl-4-hydroxy-3-oxo-3,4,4a,5,8,8a-hexahydro-1H-isochromen-7-ylmethyl ester 
• 115920-13-3 C₂₁H₂₄O₆ 
• 115920-14-4 Benzoic acid (1S,2S,6R,7S,8R,9R)-6,8-dihydroxy-10,12-dioxa-tricyclo[7.2.1.0^2,7]dodec-4-en-4-ylmethyl ester 
• 115920-11-1 C₁₄H₁₈O₅ 
• 115920-10-0 C₁₄H₁₇NO₄ 
• 113965-03-0 Acetic acid (1S,2S,6R,7S,9R)-8-oxo-10,12-dioxa-tricyclo[7.2.1.0^2,7]dodec-4-en-6-yl ester 
• 115920-12-2 C₁₄H₂₀O₅ 
• 113965-04-1 Acetic acid (1S,2S,6R,7R,8R,9R)-8-hydroxy-10,12-dioxa-tricyclo[7.2.1.0^2,7]dodec-4-en-6-yl ester 

Downstream Products

• 115944-88-2 Benzoic acid (1S,4R,4aS,5S,6S,7R,8R,8aS)-4,5,8-triacetoxy-1-acetoxymethyl-6,7-dihydroxy-3-oxo-octahydro-isochromen-7-ylmethyl ester 

Relevant academic research and scientific papers

SYNTHETIC STUDIES ON TETRODOTOXIN (1) STEREOCONTROLLED SYNTHESIS OF THE CYCLOHEXANE MOIETY

Tetrodotoxin is a potent neurotoxin, for which we planned a chemical synthesis in the optically active form.The key steps are i) Diels-Alder cycloaddition to form the optically active system with the cyclohexane moiety, ii) introduction of one-carbon frag