50707-35-2Relevant academic research and scientific papers
Novel one-step synthesis of 2-carbonyl/thiocarbonyl isoindolinones and mechanistic disclosure on the rearrangement reaction of o-phthalaldehyde with amide/thioamide analogs
Wan, Jieping,Wu, Bin,Pan, Yuanjiang
, p. 9338 - 9344 (2007)
A rearrangement reaction of o-phthalaldehyde with urea/thiourea analogs or amides/thioamides under the catalysis of TMSCl (trimethylchlorosilane) is described, whereby a series of 2-carbonyl isoindolinones and 2-thiocarbonyl isoindolinones are afforded. T
Indole-β-nucleophilic substitution. Part 9. Nitrogen nucleophiles. Syntheses of hydroxycryptolepine, cryptolepine, and quindoline
Cooper,Lovell,Joule
, p. 4283 - 4286 (2007/10/03)
The alkaloids hydroxycryptolepine, cryptolepine and quindoline have been synthesised utilising the intramolecular β-nucleophilic substitution of a 1- phenylsulfonyl-2-acylindole.
