1374399-76-4

Upstream product

• 1384957-96-3 C₁₄H₁₅NO₃ 
• 1384958-13-7 C₂₁H₂₁NO₃ 
• 1384958-00-2 C₂₀H₁₉NO₃ 
• 91569-49-2 (2-acetyl-3-indolyl)acetic acid 
• 125923-35-5 methyl (N¹-benzyl-3-indolyl)acetate 

Downstream Products

• 1374399-83-3 (R)-9-benzyl-2-[(R)-2-hydroxy-1-phenylethyl]-1-methyl-3-oxo-1,2,3,4-tetrahydropyrido[3,4-b]indole 
• 1374399-55-9 (R)-2-[(R)-2-hydroxy-1-phenylethyl]-1-methyl-1,2,3,4-tetrahydropyrido[3,4-b]indole 
• 525-40-6 (R)-1-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole 
• 142605-15-0 (1R,1'R)-9-benzyl-2-(2-hydroxy-1-phenylethyl)-1-methyl-1,2,3,4-tetrahydropyrido<3,4-b>indole 
• 1374399-78-6 (3R,11bS)-11-benzyl-11b-methyl-5-oxo-3-phenyl-3,5,6,11b-tetrahydro-2H-oxazolo[3',2':1,2]pyrido[3,4-b]indole 

Relevant academic research and scientific papers

Cyclocondensation reactions between 2-acyl-3-indoleacetic acid derivatives and phenylglycinol: Enantioselective synthesis of 1-substituted tetrahydro-β-carboline alkaloids

Cyclocondensation reactions between a variety of 2-acyl-3-indoleacetic acid derivatives and (R)-phenylglycinol were studied. Successful results were obtained from N-alkyl keto acid derivatives. The resulting tetracyclic lactams provide straightforward access to enantiopure 1-substituted tetrahydro-β- carboline alkaloids.