2003
DOI: 10.1016/s0040-4020(03)00954-2
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Efficient combination of task-specific ionic liquid and microwave dielectric heating applied to one-pot three component synthesis of a small library of 4-thiazolidinones

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Cited by 147 publications
(62 citation statements)
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“…Ionic liquid supported synthesis (ILSS) has been successfully applied for a number of organic reactions like 1,3-cycloadditions [131], Knoevengeal reaction [60], Suzuki coupling [132], synthesis of thiazolidinones [133], oligosaccharide synthesis [134], and Grieco's multicomponnet synthesis of tetrahydroquinolines [135]. Donga and coworkers described the synthesis of oligonucleotides in solution using a soluble ionic liquid support.…”
Section: Ionic Liquids As Soluble Supportsmentioning
confidence: 99%
“…Ionic liquid supported synthesis (ILSS) has been successfully applied for a number of organic reactions like 1,3-cycloadditions [131], Knoevengeal reaction [60], Suzuki coupling [132], synthesis of thiazolidinones [133], oligosaccharide synthesis [134], and Grieco's multicomponnet synthesis of tetrahydroquinolines [135]. Donga and coworkers described the synthesis of oligonucleotides in solution using a soluble ionic liquid support.…”
Section: Ionic Liquids As Soluble Supportsmentioning
confidence: 99%
“…A strategy to use task-specific ionic liquids was developed and applied to the one-pot three-component synthesis of heterocyclic compounds, together with MW irradiation [138]. Scheme 51.…”
Section: Multi-component Reactions (Mcrs) With C-cbond Formationmentioning
confidence: 99%
“…A strategy to use task-specific ionic liquids was developed and applied to the one-pot three-component synthesis of heterocyclic compounds, together with MW irradiation [138]. Imidazolium-based ILs were linked to poly(ethyleneglycol) (PEG), giving matrices to be used for the so called Ionic Liquid Phase Organic Synthesis (IoLiPOS).…”
Section: Multi-component Reactions (Mcrs) With C-cbond Formationmentioning
confidence: 99%
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“…[160], [161] While there have been multiple synthestic approaches, there is still considerable scope to develop a more environmentally friendy and efficient approach to this scaffold. [162], [163] Lingampalle et al have developed a rapid entry to 4-thiazolidinones via the N-methylpyridinium tosylate [NMP][Ts] cyclocondensation of amines, aromatic ketones, and mercaptoacetic acid. [164], [165] The reaction proceeds via imine formation, followed by rapid cyclocondensation at 120 ºC (Scheme 57).…”
Section: Crs Yielding Heterocycles With Ring Sulfur and Nitrogen Atomsmentioning
confidence: 99%