57309-13-4

Upstream product

• 1969-74-0 2-phenylisatogen 
• 676-58-4 methylmagnesium chloride 
• 73822-10-3 (2S,3R)-3-Methyl-2-phenyl-2,3-dihydro-indole-1,3-diol 
• 73822-13-6 3-methyl-2-phenyl-1H-indol-1-ol 

Downstream Products

• 73822-10-3 (2S,3R)-3-Methyl-2-phenyl-2,3-dihydro-indole-1,3-diol 
• 6011-26-3 2'-acetylbenzanilide 
• 1333823-03-2 C₂₆H₂₉N₂O₃ 
• 1333823-00-9 C₂₆H₂₉N₂O₃ 
• 1333823-07-6 C₂₆H₂₉N₂O₃ 
• 73822-19-2 C₁₅H₁₂NO 
• 73822-13-6 3-methyl-2-phenyl-1H-indol-1-ol 

Relevant academic research and scientific papers

Radical intermediates in the photorearrangement of 3-hydroxyindolic nitrones

A number of 3-hydroxy substituted indolic nitrones were found to quantitatively photorearrange to (2-benzoylamino)phenyl ketones upon UV-A irradiation. EPR-Spin Trapping experiments suggest that the process, which is believed to proceed via the formation

Stereospecific Reduction of 3-Hydroxy-3H-indoles and of their Corresponding N-Oxides with NaBH4 and LiAlH4. Synthesis of True 1-Hydroxy-2,3-disubstituted Indoles. Crystal and Molecular Structure of 3-Hydroxy-2,3-diphenylindoline

3-Hydroxy-3H-indoles (1) and their corresponding N-oxides (5) undergo stereospecific reduction at the double C=N bond giving the indoline derivatives (2) and (6) respectively, which, in acidic medium, lose water to give the 2,3-disubstituted indoles (3) and (7) whose physical and spectroscopic data are not in agreement with those reported previously.The structure of 3-hydroxy-2,3-diphenylindoline, one of the reduction products, was determined by X-ray diffraction, and it was shown that hydrogen adds at C-2 cis to the hydroxy-group on C-3. 3,3-Disubstituted-3H-indoles with two organic radicals on C-3 give a mixture of stereoisomers.