64053-78-7

Upstream product

• 118-92-3 anthranilic acid 
• 64054-23-5 2-<(tetrahidro-2-oxo-3-furanyl)amino>benzoic acid 
• 64053-80-1 1'-acetylspiroindol>-3'(1'H)-one 
• 64053-79-8 1-acetyl-4,5-dihydrospiroindole>-2,3'(1'H)-dione 

Downstream Products

• 64054-17-7 1'-p-methylbenzenesulfonylspiroindol>-3'(1'H)-one 
• 64053-93-6 1'-p-methoxybenzylspiroindol>-3'(1'H)-one 
• 64053-84-5 1'-p-chlorobenzolspiroindol>-3'(1'H)-one 

Relevant academic research and scientific papers

Stereocontrolled Synthesis of (±)-Melokhanine e via an Intramolecular Formal [3 + 2] Cycloaddition

A convergent sequence to access the indole alkaloid (±)-melokhanine E in 12-steps (8-step longest linear sequence) and an 11% overall yield is reported. The approach utilizes two cyclopropane moieties as reactive precursors to a 1,3-dipole and imine speci

Spiro[cyclopropane-1,2'-indolin]-3'-ones

Spiro[cyclopropane-1,2'-indolin]-3'-ones of the general formula: STR1 wherein the ring A is a substituted or unsubstituted phenyl ring and Z is hydrogen, a substituted or unsubstituted alkyl group or a substituted or unsubstituted acyl group and their pha