134755-35-4

Upstream product

• 134755-34-3 3,5-dibromo-4-hydroxy-β-phenethylamine 
• 73414-58-1 2-(3,5-dibromo-4-hydroxyphenyl)ethan-1-amine hydrobromide 
• 134755-33-2 6-methoxy-3-<2-<<<2-(trimethylsilyl)ethoxy>carbonyl>amino>ethyl>indole-4,7-dione 
• 32884-23-4 2-benzyloxy-4-methoxybenzaldehyde 
• 138518-19-1 (4-Benzyloxy-6-methoxy-1H-indol-3-ylmethyl)-trimethyl-ammonium; iodide 
• 134755-32-1 4-(benzyloxy)-6-methoxy-3-<2-<<<2-(trimethylsilyl)ethoxy>carbonyl>amino>ethyl>indole 
• 134755-22-9 ethyl 4-(benzyloxy)-6-methoxyindole-2-carboxylate 
• 143878-19-7 [2-(4-Hydroxy-6-methoxy-1H-indol-3-yl)-ethyl]-carbamic acid 2-trimethylsilanyl-ethyl ester 
• 134755-23-0 <4-(benzyloxy)-6-methoxy-3-indolyl>acetonitrile 
• 138518-15-7 4-(benzyloxy)-6-methoxyindole-2-carboxylic acid 
• 143878-17-5 2-(4-Benzyloxy-6-methoxy-1H-indol-3-yl)-ethylamine 
• 138540-76-8 6-methoxy-4-phenylmethoxy-N,N-dimethyl-3-(1H)-indolemethanamine 
• 138518-16-8 4-benzyloxy-6-methoxy-1H-indole 
• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 

Relevant academic research and scientific papers

Total synthesis of discorhabdin C: A general aza spiro dienone formation from O-silylated phenol derivatives using a hypervalent iodine reagent

Hypervalent iodine oxidation of O-silylated phenols bearing various types of aminoquinones at the para position in 2,2,2-trifluoroethanol gave azacarbocyclic spiro dienones in good yields. Using this method, the first total synthesis of discorhabdin C, wh

Hypervalent iodine oxidation of O-silylated phenol derivatives to azacarbocyclic spirodienones; synthetic approach to the anticancer marine alkaloid, discorhabdin C

Hypervalent iodine oxidation of O-silylated phenols bearing various types of aminoquinones at the p-position in 2,2,2-trifluoroethanol gave azacarbocyclic spirodienones in good yields and application of this reaction to the synthetic approach to discorhab