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Iodine-catalysed synthesis of thiopyrano[3,4-c]quinoline derivatives via imino-Diels-Alder reaction

A mild and efficient method for the synthesis of thiopyrano[3,4-c]quinoline derivatives via an imino-Diels-Alder reaction of an aromatic aldehyde, 5-amino-1H-indazole or 2-aminoanthracene and tetrahydrothiopyran-4-one catalysed by iodine is described. This new procedure has the advantages of mild re... Full description

Journal Title: Journal of Chemical Research Jun 2012, Vol.36(6), pp.318-321
Main Author: Wang, Wei
Other Authors: Yin, Ming-Yue , Zhang, Mei-Mei , Wang, Xiang-Shan
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: ISSN: 1747-5198 ; E-ISSN: 2047-6507 ; DOI: 10.3184/174751912X13352797144052
Link: http://search.proquest.com/docview/1494356717/?pq-origsite=primo
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title: Iodine-catalysed synthesis of thiopyrano[3,4-c]quinoline derivatives via imino-Diels-Alder reaction
format: Article
creator:
  • Wang, Wei
  • Yin, Ming-Yue
  • Zhang, Mei-Mei
  • Wang, Xiang-Shan
subjects:
  • Aldehydes
  • Chemical and Electrochemical Properties (MD)
  • Chemical and Electrochemical Properties (Ep)
  • Chemical and Electrochemical Properties (Ed)
  • Chemical and Electrochemical Properties (EC)
ispartof: Journal of Chemical Research, Jun 2012, Vol.36(6), pp.318-321
description: A mild and efficient method for the synthesis of thiopyrano[3,4-c]quinoline derivatives via an imino-Diels-Alder reaction of an aromatic aldehyde, 5-amino-1H-indazole or 2-aminoanthracene and tetrahydrothiopyran-4-one catalysed by iodine is described. This new procedure has the advantages of mild reaction conditions, high yields and metalfree catalysis. This is useful since quinoline and its derivatives have extensive biological activities.
language: eng
source:
identifier: ISSN: 1747-5198 ; E-ISSN: 2047-6507 ; DOI: 10.3184/174751912X13352797144052
fulltext: no_fulltext
issn:
  • 17475198
  • 1747-5198
  • 20476507
  • 2047-6507
url: Link


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titleIodine-catalysed synthesis of thiopyrano[3,4-c]quinoline derivatives via imino-Diels-Alder reaction
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subjectAldehydes ; Chemical and Electrochemical Properties (MD) ; Chemical and Electrochemical Properties (Ep) ; Chemical and Electrochemical Properties (Ed) ; Chemical and Electrochemical Properties (EC)
descriptionA mild and efficient method for the synthesis of thiopyrano[3,4-c]quinoline derivatives via an imino-Diels-Alder reaction of an aromatic aldehyde, 5-amino-1H-indazole or 2-aminoanthracene and tetrahydrothiopyran-4-one catalysed by iodine is described. This new procedure has the advantages of mild reaction conditions, high yields and metalfree catalysis. This is useful since quinoline and its derivatives have extensive biological activities.
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descriptionA mild and efficient method for the synthesis of thiopyrano[3,4-c]quinoline derivatives via an imino-Diels-Alder reaction of an aromatic aldehyde, 5-amino-1H-indazole or 2-aminoanthracene and tetrahydrothiopyran-4-one catalysed by iodine is described. This new procedure has the advantages of mild reaction conditions, high yields and metalfree catalysis. This is useful since quinoline and its derivatives have extensive biological activities.
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titleIodine-catalysed synthesis of thiopyrano[3,4-c]quinoline derivatives via imino-Diels-Alder reaction
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abstractA mild and efficient method for the synthesis of thiopyrano[3,4-c]quinoline derivatives via an imino-Diels-Alder reaction of an aromatic aldehyde, 5-amino-1H-indazole or 2-aminoanthracene and tetrahydrothiopyran-4-one catalysed by iodine is described. This new procedure has the advantages of mild reaction conditions, high yields and metalfree catalysis. This is useful since quinoline and its derivatives have extensive biological activities.
doi10.3184/174751912X13352797144052
urlhttp://search.proquest.com/docview/1494356717/
date2012-06