95646-55-2Relevant academic research and scientific papers
Facile creation of 2-substituted indolin-3-ones by using primary-secondary diamine catalysts
Sun, Wangsheng,Hong, Liang,Wang, Rui
supporting information; experimental part, p. 6030 - 6033 (2011/06/22)
Indolin-3-ones with a chiral center at the 2-position are encountered in a large variety of natural products and can be used in the total synthesis of biologically active alkaloids such as (+)-austamide, (-)-brevianamideB, (+)-aristotelone, isatisineA, an
NEW METHOD OF SYNTHESIS OF QUINDOLINES FROM 1,5-DIKETONES OF THE INDOLINONE SERIES
Sevodin, V. P.,Velezheva, V. S.,Erofeev, Yu. V.,Suvorov, N. N.
, p. 1374 - 1380 (2007/10/02)
By the action of ammonium acetate and α,β-unsaturated carbonyl compounds, 1,5-diketones of the indolinone series undergo not yet known transformations into difficulty accessible 1,2-dihydro-10H-quindolines.Under these conditions, 11-phenyl-1,2,3,4-tetrahydro-10H-quindoline was obtained from 1-acetyl-2-(benzylcyclohexan-1-on-α-yl)indolin-3-one.Dihydroquindolines with identical aryl substituents in the 1- and 11-positions were obtained from 1-acetylindolin-3-one by the action of an excess of certain α,β-unsaturated ketones and ammonium acetate.Dehydrogenation ofdihydroquindolines proceeds smoothly on heating with sulfur.The possible paths of the formation of dihydroquindolines are discussed.
