2021
DOI: 10.1021/acs.orglett.1c00866
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On the Enantioselective Phosphoric-Acid-Catalyzed Hantzsch Synthesis of Polyhydroquinolines

Abstract: HAL is a multi-disciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers. L'archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d'enseignement et de recherche français ou étrangers, des labor… Show more

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Cited by 11 publications
(3 citation statements)
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“…of dimedone is heated with aldehyde derivatives in the presence of ethyl acetoacetate and an ammonia source. [1][2][3] In this sense, a multi-step sequence ensues, a water molecule is lost and the target sixmembered nitrogen-containing scaffold is formed. 4,5 It possesses a chiral center at the phenyl-substituted carbon.…”
Section: Introductionmentioning
confidence: 99%
“…of dimedone is heated with aldehyde derivatives in the presence of ethyl acetoacetate and an ammonia source. [1][2][3] In this sense, a multi-step sequence ensues, a water molecule is lost and the target sixmembered nitrogen-containing scaffold is formed. 4,5 It possesses a chiral center at the phenyl-substituted carbon.…”
Section: Introductionmentioning
confidence: 99%
“…These chemicals have been shown to have a variety of medicinal functions, [30–34] including neuroprotectant, [35] platelet anti‐aggregatory action, [36–38] cerebral antischemic activity [39] in the treatment of Alzheimer's disease, [40] and as chemosensitizer in tumour therapy [41] . These examples show the extraordinary potential of dihydropyridine (polyhydroquinoline) derivatives as a source of promising therapeutic candidates [42–44] . In addition, the oxidation of these compounds to pyridines has been thoroughly investigated.…”
Section: Introductionmentioning
confidence: 99%
“…[41] These examples show the extraordinary potential of dihydropyridine (polyhydroquinoline) derivatives as a source of promising therapeutic candidates. [42][43][44] In addition, the oxidation of these compounds to pyridines has been thoroughly investigated. As a result, the synthesis of this heterocyclic nucleus is crucial.…”
Section: Introductionmentioning
confidence: 99%