88901-86-4

Upstream product

• 15741-79-4 N-benzyl tryptamine 
• 136945-86-3 3-C-(carboxy-methylene)-2,3-didesoxy-α-β-D-erythro-pentapyranose 
• 134747-17-4 methyl 3-C-(carboxymethylene)-2,3-didesoxy-α-D-ribo-hexapyranoside-2',4-γ-lactone 
• 88901-92-2 methyl 4,6-O-benzylidene-3-C-(carbomethoxy-methylene)-2,3-didesoxy-α-D-ribo-hexapyranoside 
• 88901-93-3 methyl 3-C-(carbomethoxy-methylene)-2,3-didesoxy-α-β-D-erythro-hexafuranoside 
• 88901-94-4 methyl 3-C-(carbomethoxy-methylene)-2,3-didesoxy-α-β-D-erythro-pentafuranoside 
• 136945-85-2 methyl 3-C-(carbomethoxy-methylene)-2,3-didesoxy-5-aldehydo-α-β-D-erythro-pentafuranoside 

Downstream Products

• 88930-21-6 C₂₄H₂₅N₂O₂⁽¹⁺⁾*C₇H₇O₃S^(1-) 

Relevant academic research and scientific papers

An Approach to the Chiral Synthesis of Heteroyohimbine Alkaloids

Methyl α-D-mannopyranoside is used as a chiral starting material to prepare two epimeric substituted indoloquinolizidines which could serve as chiral synthons for the total synthesis of (-)ajmalicine (1) and the heteroyohimbine alkaloids in general