1213-48-5Relevant articles and documents
Study of the addition of Grignard reagents to 2-aryl-3H-indol-3-ones
Liu, Yahua,McWhorter Jr., William W.
, p. 2618 - 2622 (2007/10/03)
Grignard reagents are added to the carbonyl group of 2-aryl-3H-indol-3-ones to generate 3-alkyl-(or phenyl)-2-aryl-3H-indol-3-ols, which are in turn rearranged to yield 2-alkyl(or phenyl)-2-aryl-1,2-dihydro-3H-indol-3-ones.
New Aspects in the Chlorination of Indoles with 1-Chlorobenzotriazole and 1-Chloroisatin
Berti, C.,Greci, L.,Andruzzi, R.,Trazza, A.
, p. 4895 - 4899 (2007/10/02)
2-Phenyl-, 1-methyl-2-phenyl-, and 2-phenyl-3-methylindole react with 1-chlorobenzotriazole and 1-chloroisatin to form essentially 3-chloroindoles.The composition of the products, which depends on the solvent used, suggests an electron-transfer process fo
THE REARRANGEMENT OF HYDROPEROXYINDOLENINES
McCapra, F.,Long, P. V.
, p. 3009 - 3012 (2007/10/02)
Examination of a series of substituted 3-(hydroxyperoxy)indolenines favours a mechanism for base catalysed decomposition of the dioxetan rather than Criegee type.