320748-66-1

Upstream product

• 171523-63-0 <2S-(2β,3aβ,7aβ)>-2,3,3a,6,7,7a-hexahydro-3a-benzoyloxy-6-oxo-1H-indole-1,2-dicarboxylic acid 1-benzyl 2-methyl ester 
• 144534-49-6 (2S,3aR,7aR)-3a-hydroxy-6-oxo-2,3,3a,6,7,7a-hexahydroindole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 320748-65-0 (2S,3aS,7aS)-3a-(benzoyloxy)-6-oxo-2,3,3a,6,7,7a-hexahydroindole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 

Downstream Products

• 320748-89-8 C₇₃H₁₂₂N₆O₁₁Si₄ 
• 320748-86-5 C₇₃H₁₂₂N₆O₁₁Si₄ 
• 320748-85-4 C₄₇H₇₃N₅O₉Si₂ 
• 320748-70-7 (2S,3aS,6R,7aS)-6-(tert-butyldimethylsiloxy)-2,3,3a,4,5,6,7,7a-octahydroindole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 320748-68-3 1-benzyl 2-methyl (2S,3aS,6S,7aS)-6-hydroxyoctahydro-1H-indole-1,2-dicarboxylate 
• 320748-69-4 (2S,3aS,6R,7aS)-6-hydroxy-2,3,3a,4,5,6,7,7a-octahydroindole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 320748-67-2 (2S,3aS,7aS)-6-oxo-2,3,3a,4,5,6,7,7a-octahydroindole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 

Relevant academic research and scientific papers

Asymmetric synthesis of common aza-tricyclic core of various alkaloids

The asymmetric synthesis of common aza-tricyclic core of different types of natural alkaloids had been accomplished from commercially available l-Cbz-tyrosine. This practical approach was capable of generating scale-up aza-tricyclic skeleton. Meanwhile, i

Total synthesis and stereochemical revision of (+)-aeruginosin 298-A.

[structure:see text] Novel routes toward both enantiomers of the bicyclic proline surrogate 2-carboxy-6-hydroxyoctahydroindole, i.e., Choi, were developed on the basis of the oxidative cyclization of L-tyrosine. Synthesis of the proposed sequence of (+)-a