Zobrazeno 1 - 10
of 213
pro vyhledávání: '"Rolf H. Prager"'
Publikováno v:
ARKIVOC, Vol 2001, Iss 7, Pp 88-103 (2001)
Externí odkaz:
https://doaj.org/article/898cbe32ab3c4b2bbca0fcc9124e55ab
Publikováno v:
Arkivoc. 2020:117-152
Publikováno v:
Journal of Chemical Reviews. 1:233-242
This review provides an overview of the recent literature on application of arylglyoxals the synthesis of pyrrolo[2,3-d]pyrimidines via multicomponent reactions in the period of 2008–2018. 1,2-Dicarbonyl compounds are attractive precursors for synt
Publikováno v:
Bulletin of the Chemical Society of Ethiopia.
A convenient and efficient synthesis of new bis -quinoxaline is described, involving condensation of 1,2-diamines with 9-ethyl-3,6-di(1,2-dioxoethyl)carbazole in the presence of Tonsil clay, a readily available and inexpensive catalyst. The structure
Publikováno v:
Tetrahedron Letters. 57:105-109
A mild and efficient method for the chemoselective synthesis of 7-aryloyl-5 H -pyrano[3,2- c :5,6- c ′]diquinoline-6,8(7 H ,9 H )-diones, representing a new class of substituted pyranodiquinolinone derivatives, via the annulation of arylglyoxalmono
Publikováno v:
ChemInform. 47
A mild and efficient method for the chemoselective synthesis of 7-aryloyl-5 H -pyrano[3,2- c :5,6- c ′]diquinoline-6,8(7 H ,9 H )-diones, representing a new class of substituted pyranodiquinolinone derivatives, via the annulation of arylglyoxalmono
Publikováno v:
Bulletin of the Korean Chemical Society. 33:2890-2896
A simple regioselective synthesis of cinnoline derivatives was achieved by a one-pot three component synthetic methodology. New substituted 7,8-dihydrocinnolin-5(6H)-ones are prepared via one-pot three component reaction of arylglyoxals with 1,3-cycl
Publikováno v:
Chemistry of Heterocyclic Compounds. 48:931-935
Several new derivatives of imidazo[1,2-a]quinoxalines have been synthesized in good to excellent yields starting from arylaminoisoxazol-5(2H)-ones and 2,3-dichloroquinoxaline through a rearrangement under mild base-catalyzed conditions.
Publikováno v:
Bulletin of the Korean Chemical Society. 32:2183-2186
A series of pyrimidoquinoline derivatives was synthesized in good yield and short reaction times by reaction of 3-arylaminoisoxazol-5(2H)-ones with derivatives of 2-chloro-3-formylquinoline in toluene under reflux conditions.
Publikováno v:
Australian Journal of Chemistry. 71:435
A novel and one-pot pseudo-four-component reaction between a series of arylglyoxals, malononitrile, 3-methyl-1-phenyl-1H-pyrazol-5-amine, and acetone in the presence of tetrapropylammonium bromide (TPAB) has been developed to synthesize a series of n