91444-16-5

Upstream product

• 536-90-3 m-Anisidine 
• 104598-83-6 1-benzyl-6-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole 
• 52351-75-4 6-methoxyisatin 
• 487003-20-3 1-benzyl-6-methoxy-1H-indole-2,3-dione 
• 21086-33-9 2-bromo-1-(4-methoxyphenyl)-1-propanone 

Downstream Products

• 104599-17-9 2-(4-Hydroxy-phenyl)-3-methyl-1-phenyl-1H-indol-6-ol 
• 104599-01-1 1-Benzyl-2-(4-hydroxy-phenyl)-3-methyl-1H-indol-6-ol 
• 104599-35-1 Acetic acid 2-(4-acetoxy-phenyl)-3-methyl-1-phenyl-1H-indol-6-yl ester 
• 104599-19-1 Acetic acid 2-(4-acetoxy-phenyl)-1-benzyl-3-methyl-1H-indol-6-yl ester 
• 86111-15-1 1-Ethyl-2-(4-hydroxy-phenyl)-3-methyl-1H-indol-6-ol 
• 86111-14-0 2-(4-Hydroxy-phenyl)-1,3-dimethyl-1H-indol-6-ol 
• 91444-56-3 2-(4-Hydroxy-phenyl)-1-isopropyl-3-methyl-1H-indol-6-ol 
• 86111-16-2 2-(4-Hydroxy-phenyl)-3-methyl-1-propyl-1H-indol-6-ol 
• 91444-50-7 Acetic acid 2-(4-acetoxy-phenyl)-3-methyl-1H-indol-6-yl ester 
• 86111-29-7 Acetic acid 2-(4-acetoxy-phenyl)-1,3-dimethyl-1H-indol-6-yl ester 
• 86111-30-0 Acetic acid 2-(4-acetoxy-phenyl)-1-ethyl-3-methyl-1H-indol-6-yl ester 
• 91444-57-4 Acetic acid 2-(4-acetoxy-phenyl)-1-isopropyl-3-methyl-1H-indol-6-yl ester 
• 86111-31-1 Acetic acid 2-(4-acetoxy-phenyl)-3-methyl-1-propyl-1H-indol-6-yl ester 
• 158611-24-6 6-methoxy-2-(4-methoxyphenyl)-1H-indole-3-carbaldehyde 

Relevant academic research and scientific papers

Divergent and Orthogonal Approach to Carbazoles and Pyridoindoles from Oxindoles via Indole Intermediates

The previously unexplored Grignard addition to oxindoles provides a regiospecific approach to 2- and 2,3-disubstituted indole derivatives in high yields via a one-pot aromatization driven dehydration pathway. This method allows a convenient preparation of diallyl indoles that are used as ring-closing metathesis (RCM) precursors for the orthogonal synthesis of pyrido[1,2-a]indoles and carbazoles. The synthetic utility of this method is illustrated by the synthesis of a microtubulin inhibitor and naturally occurring carbazole alkaloids.

2-Phenylindoles. Relationship between Structure, Estrogen Receptor Affinity, and Mammary Tumor Inhibiting Activity in the Rat

A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized.In addition, different alkyl groups were introduced into positions