2003
DOI: 10.1002/ejoc.200300378
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Pd‐Assisted Multicomponent Synthesis of Heterocycles

Abstract: This review highlights some remarkable recently made achievements in the application of palladium‐mediated processes to the design of multicomponent one‐pot syntheses of heterocyclic compounds. Palladium‐catalysed cascade reactions are surveyed, together with processes based on sequential, one‐pot performance of individual transformations in which at least one is catalysed by palladium. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

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Cited by 469 publications
(112 citation statements)
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“…[1][2][3][4][5][6] One-pot reactions increase the efficiency of reactants by combing several operational steps without isolation of intermediates or changing the reaction conditions. Speed, diversity, efficiency and environmental amiability are some of the major advantages of these reactions.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6] One-pot reactions increase the efficiency of reactants by combing several operational steps without isolation of intermediates or changing the reaction conditions. Speed, diversity, efficiency and environmental amiability are some of the major advantages of these reactions.…”
Section: Introductionmentioning
confidence: 99%
“…Due to numerous advantages, these heavy compound molecules synthesized by the reaction of small molecule. Biginelli reaction is one of MCR that considerable attention recently 1 .…”
Section: Introductionmentioning
confidence: 99%
“…Multicomponent reactions (MCRs) [1][2][3][4][5] in general and isocyanide-based multicomponent reactions (IMCRs) [6][7][8][9][10] in particular have attracted the attention of chemist's during the past years. These reactions are well defined and suited for combinational library synthesis due to the fact that products are formed in one-pot reactions [11][12].…”
Section: Introductionmentioning
confidence: 99%