1298035-48-9

Upstream product

• 151721-32-3 N-benzenesulfonyl-o-aminobenzaldehyde 
• 299-26-3 1-(1H-indol-3-yl)propan-2-amine 
• 100-52-7 benzaldehyde 
• 2900-27-8 2-(tert-butoxycarbonylamino)-2-phenylacetic acid 
• 615-43-0 2-iodophenylamine 
• 1298035-43-4 tert-butyl 2-(2-iodophenylamino)-2-oxo-1-phenylethylcarbamate 
• 1132839-71-4 C₁₄H₁₃IN₂O 
• 1298035-47-8 N-(2-iodophenyl)-2-methyl-4-phenyloxazol-5-amine 
• 7486-35-3 tri-n-butyl(vinyl)tin 

Relevant academic research and scientific papers

Cu-catalyzed mild and efficient oxidation of THβCs using air: Application in practical total syntheses of perlolyrine and flazin

A mild, efficient and environmentally benign method for synthesis of aromatic β-carbolines via Cu(ii)-catalyzed oxidation of 1,2,3,4-tetrahydro-β-carbolines (THβCs) was developed, in which air (O2) was used as the clean oxidant. This method has advantages such as environmentally friendliness, mildness, very good tolerance of functional groups, high yielding and easy experiment operation. In addition, this new methodology was successfully applied in the efficient and practical total syntheses of β-carboline alkaloids perlolyrine and flazin.

A short divergent approach to highly substituted carbazoles and β-carbolines via in situ-generated diketoindoles

Based on an aza-alkylation/Michael addition cascade reaction developed by Kim and co-workers we have developed divergent cascade reactions leading to either highly substituted 1-hydroxycarbazoles, 3-hydroxycarbazoles or β-carbolines, starting from readily

Intramolecular [4+2]-cycloaddition of 5-amino-substituted oxazoles as an approach toward the left-hand segment of haplophytine

The [4+2]-cycloaddition chemistry of several 5-amino-substituted oxazoles has been examined as an approach toward the construction of the left-half segment of the aspidosperma alkaloid haplophytine. Georg Thieme Verlag Stuttgart.