943144-60-3

Upstream product

• 943144-59-0 (2R,3S,4Z)-3-ethyl-2,6-bis(4-methoxybenzyloxy)-4-hexen-1-ol 
• 149-30-4 2-Mercaptobenzothiazole 
• 1576-96-1 (E)-2-penten-1-ol 
• 104530-72-5 ((2S,3S)-3-ethyloxiran-2-yl)methanol 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 943144-58-9 C₂₄H₃₀O₅ 
• 943144-57-8 (2R,3S)-3-ethyl-1,2-(4-methoxybenzylidenedioxy)-6-(4-methoxybenzyloxy)-4-hexyne 
• 943144-56-7 (2R,3S)-3-ethyl-6-(4-methoxybenzyloxy)-4-hexyne-1,2-diol 

Downstream Products

• 943144-53-4 (2R,3S,4Z)-1-(benzothiazole-2-sulfonyl)-3-ethyl-2,6-bis(4-methoxybenzyloxy)-4-hexene 
• 467234-66-8 (S)-6-Methyl-octanoic acid (1S,3R)-3-[(1Z,3Z,9E)-(5R,7R,8R)-8-(2-allyloxycarbonylamino-ethyl)-10-((2S,3S)-3-ethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-5,7,8-trihydroxy-deca-1,3,9-trienyl]-cyclohexyl ester 
• 145142-82-1 leustroducsin B 
• 943144-83-0 (5S,6S)-6-[(1E,3R,4R,6R,7Z,9Z)-3-[2-(allyloxycarbonylamino)ethyl]-6-tert-butyldimethylsiloxy-3,4-dihydroxy-10-[(1R,3S)-3-[(6S)-methyloctanoyloxy]cyclohexyl]-1,7,9-decatrienyl]-5-ethyl-5,6-dihydro-2H-pyran-2-one 
• 943144-77-2 C₄₂H₆₁IO₆Si₂ 
• 943144-76-1 C₄₁H₆₀O₇Si₂ 
• 943144-75-0 (2R,4R,5R,6E,8S,9S,10Z)-2-tert-butyldimethylsiloxy-5-(2-tert-butyldiphenylsiloxyethyl)-9-ethyl-4,5-isopropylidenedioxy-6,10-dodecadiene-1,8,12-triol 
• 943144-74-9 (2R,4R,5R,6E,8S,9S,10Z)-2-tert-butyldimethylsiloxy-5-(2-tert-butyldiphenylsiloxyethyl)-9-ethyl-4,5-isopropylidenedioxy-8,12-bis(4-methoxybenzyloxy)-6,10-dodecadiene 

Relevant academic research and scientific papers

Total synthesis of leustroducsin B

(Chemical Equation Presented) Leustroducsin B was synthesized via a convergent route based on division of the leustroducsin molecule into three segments A, B, and C. Two coupling reactions (Julia coupling reaction and Nozaki-Hiyama-Kishi (NHK) reaction) w

Total synthesis of leustroducsin B via a convergent route

Total synthesis of leustroducsin B was achieved via a convergent route, which includes Julia coupling reaction of segment A with segment B followed by Stille coupling reaction of segment C.