26487-02-5

Upstream product

• 1062261-30-6 ethyl 2-(azidomethyl)benzoate 
• 7647-01-0 hydrogenchloride 
• 136918-14-4 phthalimide 
• 64-17-5 ethanol 
• 7732-18-5 water 
• 7468-67-9 o-formylbenzonitrile 
• 26486-93-1 3-hydroxy-2,3-dihydro-isoindol-1-one 

Downstream Products

• 93679-79-9 3-phenethylamino-isoindolin-1-one 
• 93679-80-2 3-p-toluidino-isoindolin-1-one 
• 123783-98-2 (2R,3S,9bR)-3-Methyl-2-phenethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-98-2 (2R,3R,9bR)-3-Methyl-2-phenethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-99-3 (2R,3S,9bR)-2-Benzyl-3-methyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-99-3 (2R,3R,9bR)-2-Benzyl-3-methyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-85-7 3-((E)-3-Phenyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 98289-81-7 (3S,9bR)-3-Ethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 98289-81-7 (3R,9bR)-3-Ethyl-2,3-dihydro-9bH-oxazolo[2,3-a]isoindol-5-one 
• 123783-92-6 (S)-3-((R)-1-Phenethyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-92-6 (S)-3-((S)-1-Phenethyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-93-7 (S)-3-((R)-1-Benzyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-93-7 (S)-3-((S)-1-Benzyl-allyloxy)-2,3-dihydro-isoindol-1-one 
• 123783-84-6 3-((Z)-3-Phenyl-allyloxy)-2,3-dihydro-isoindol-1-one 

Relevant academic research and scientific papers

One-pot synthesis of 3-alkoxy-2,3-dihydro-1H-isoindol-1-ones by the reactions of 2-(Azidomethyl)benzoates with NaH

Abstract A new and facile method for the general preparation of 3-alkoxy-2,3-dihydro-1H-isoindol-1-ones has been developed. Thus, the reaction of 2-(azidomethyl)benzoates with NaH affords, after workup with H2O, 3-alkoxy-2,3-dihydro-1H-isoindol

A REMOVABLE AUXILIARY FOR AMIDOMERCURATION REACTIONS: THE STEREOCONTROLLED PREPARATION OF VICINAL AMINOALCOHOLS

Unsaturated amidals 1, derived from allylic alcohols and containing a stereogenic amidal center, undergo amidomercuration with high 1,3-stereoinduction from the amidal center.In substrates derived from secondary allylic alcohols, the influence of the ster

Synthesis of Isoindoles. Acid or Base Induced Cyclization of 2-Cyanobenzaldehyde with Alcohols

Various 3,3-dialkoxy-2,3-dihydro-1-hydroxy-1H-isoindoles (2) were obtained by treating 2-cyanobenzaldehyde (1) with alcohols in the presence of an acid catalyst such as silica gel.In the reaction using a base catalyst such as triethylamine and 1,8-diazabi