luotonin-a and tryptanthrine

luotonin-a has been researched along with tryptanthrine* in 2 studies

Other Studies

2 other study(ies) available for luotonin-a and tryptanthrine

ArticleYear
One-pot synthesis of simple alkaloids: 2,3-polymethylene-4(3H)-quinazolinones, luotonin A, tryptanthrin, and rutaecarpine.
    Chemical & pharmaceutical bulletin, 2008, Volume: 56, Issue:4

    One-pot synthesis of various 2,3-polymethylene-4(3H)-quinazolinones from anthranilic acid, corresponding lactam and SOCl(2) is described, which can be applicable to the synthesis of simple 4(3H)-quinazolinone-derived alkaloids, such as luotonin A, tryptanthrin, and rutaecarpine.

    Topics: Chemical Phenomena; Chemistry, Physical; Indicators and Reagents; Indole Alkaloids; Lactams; Magnetic Resonance Spectroscopy; ortho-Aminobenzoates; Pyrroles; Quinazolines; Quinazolinones; Quinones; Spectrophotometry, Infrared

2008
Radical reactions with 3H-quinazolin-4-ones: synthesis of deoxyvasicinone, mackinazolinone, luotonin A, rutaecarpine and tryptanthrin.
    Organic & biomolecular chemistry, 2007, Jan-07, Volume: 5, Issue:1

    Alkyl, aryl, heteroaryl and acyl radicals have been cyclised onto the 2-position of 3H-quinazolin-4-one. The side chains containing the radical precursors were attached to the nitrogen atom in the 3-position. The cyclisations take place by aromatic homolytic substitution hence retain the aromaticity of the 3H-quinazolin-4-one ring. The highest yields were obtained using hexamethylditin to facilitate cyclisation rather than reduction without cyclisation. The alkaloids deoxyvasicinone , mackinazolinone , tryptanthrin , luotonin A and rutaecarpine were synthesised by radical cyclisation onto 3H-quinazolin-4-one.

    Topics: Alkaloids; Cyclization; Free Radicals; Indole Alkaloids; Molecular Structure; Pyrroles; Quinazolines; Quinazolinones; Quinones

2007