One-pot multi-component reaction

Heravi MM, Baghemejad B, Oskooie HA, Hekmatshoar R (2008) A novel and facile synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl-lH-indole (5H)-ones via a one-pot multi-component reaction. Tetrahedron Lett 49 6101-6103... [Pg.275]

In the first part of this one-pot multi-component reaction a carbonyl group reacts with a CH-acidic compound. [Pg.110]

Wu and co-workers described a novel one-pot multi-component reaction between 2-alkynylbenzaldehydes 129, amines 130 and ketones 131 catalyzed by AgOTf and proline to give 1,2-dihydroisoquinolines 132 <07OL4959>. [Pg.309]

Zhu SL, Ji SJ, Su XM et al (2008) Facile and efficient synthesis of a new class of bis(3 -indolyl) pyridine derivatives via one-pot multi-component reactions. Tetrahedron Lett 49 1777-1781... [Pg.224]

Zhu S-L, Zhao K, Su X-M et al (2009) Microwave-assisted synthesis of new spiro[indoline-3, 4 -quinoline] derivatives via a one-pot multi-component reaction. Synth Commun 39 1355-1366... [Pg.227]

X. Zhang, X. Li, X. Fan, X. Wang, D. Li, G. Qu, J. Wang, Mol. Divers. 2009,13, 57-61. Ionic liquid promoted preparation of 4/f-thiopyran and pyrimidine nucleoside-thiopyran hybrids through one-pot multi-component reaction of thioamide. [Pg.380]

Type of reaction C-N bond formation Reaction conditions Acetonitrile, room temperature Synthetic strategy One-pot multi-component reaction Catalyst Triphenylphospine (Ph3P)... [Pg.125]

Keywords Aromatic aldehydes, anilines, triethylphosphite, TiOa-nanoparticles, solvent-free, room temperature, one-pot multi-component reaction, a-aminophosphonates... [Pg.285]

One-pot multi-component reaction (MCR) involving a new environment-friendly catalytic procedure has been developed for the S5mthesis of benzimidazoles [120]. The alcohol oxidation is combined with further formation of imidazoline ring, wherein each product becomes the substrate for the next reaction. The one-pot reactions are controlled by means of the sequential addition of diamines after ensuring the almost complete consumption of the... [Pg.245]

Similar substituted quinolines can be efficiently obtained starting from N-alltylaniline (including glycine) derivatives by reaction with alkenes in the presence of FeCls (10 mol%) and TEMPO oxoammonium tetrafluoroborate salt (2 equiv.) as the oxidant in dichloromethane (DCM) at 60 °C. Interestingly, the same quinolines can be obtained starting from anilines, ethyl glyoxalate and alkenes, in a one-pot multi-component reaction, under similar conditions. ... [Pg.84]

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