109748-83-6

Upstream product

• 109740-20-7 C₅₈H₆₆N₄O₁₁S 
• 4124-41-8 p-toluenesulfonylanhydride 
• 109704-68-9 N^b-benzyl-20-(3-hydroxypropyl)-D-nordesethylvincadifformine 
• 109704-69-0 Nβ-benzyl-20-<3-(p-toluenesulfonyloxy)propyl>-20-desethyl-D-norvincadifformine 
• 109704-70-3 (3aS,4R,11bR)-3-Benzyl-6-chloro-4-[3-(toluene-4-sulfonyloxy)-propyl]-2,3,3a,4,5,6-hexahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylic acid methyl ester 
• 110222-32-7 methyl 3-benzyl-1,2,3,4,5,6,7,8-octahydro-5(3-p-toluenesulfonyloxypropyl)azonino (6,7-b)indole-7-carboxylate 
• 126572-48-3 (Z)-7-Benzyl-4b-chloro-9-[3-(toluene-4-sulfonyloxy)-propyl]-4b,5,6,7,8,9,10,12-octahydro-7,12-diaza-cyclonona[a]indene-11-carboxylic acid methyl ester 
• 5826-69-7 vindoline hydrochloride 

Downstream Products

• 109704-74-7 C₅₁H₆₁N₄O₈⁽¹⁺⁾*C₇H₇O₃S^(1-) 
• 109704-74-7 C₅₁H₆₁N₄O₈⁽¹⁺⁾*C₇H₇O₃S^(1-) 
• 109704-74-7 C₅₁H₆₁N₄O₈⁽¹⁺⁾*C₇H₇O₃S^(1-) 
• 109704-74-7 C₅₁H₆₁N₄O₈⁽¹⁺⁾*C₇H₇O₃S^(1-) 

Relevant academic research and scientific papers

Three Routes to the Critical C16'-C14' Parf Relative Stereochemistry of Vinblastine. Syntheses of 20'-Desethyl-20'-deoxyvinblastine and 20'-Desethyl-20'-deoxyvincovaline

Coupling reactions of vindoline (2) with the racemic chloro imine derivative 8 of 14-epi-D-secodesethylvincadifformine (7) resulted in a selective high yield formation of the C16'-C14' parf (vinblastine type) relative configuration of the coupling product