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The De Kimpe azirdine synthesis is a name reaction of organic chemistry, for the generation of aziridines by the reaction of α-chloroimines with nucleophiles such as hydride, cyanide, or Grignard reagents. The De Kimpe aziridine synthesis is suitable for both aldimines and ketamines, particularly those with two alkyl substituents on the α-carbon (Thorpe-Ingold effect).

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  • The De Kimpe azirdine synthesis is a name reaction of organic chemistry, for the generation of aziridines by the reaction of α-chloroimines with nucleophiles such as hydride, cyanide, or Grignard reagents. The De Kimpe aziridine synthesis is suitable for both aldimines and ketamines, particularly those with two alkyl substituents on the α-carbon (Thorpe-Ingold effect). (en)
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  • 66568992 (xsd:integer)
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  • 2418 (xsd:nonNegativeInteger)
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  • 1116698317 (xsd:integer)
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dbp:name
  • De Kimpe aziridine synthesis (en)
dbp:namedafter
  • Norbert De Kimpe (en)
dbp:type
  • Ring forming reaction (en)
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  • The De Kimpe azirdine synthesis is a name reaction of organic chemistry, for the generation of aziridines by the reaction of α-chloroimines with nucleophiles such as hydride, cyanide, or Grignard reagents. The De Kimpe aziridine synthesis is suitable for both aldimines and ketamines, particularly those with two alkyl substituents on the α-carbon (Thorpe-Ingold effect). (en)
rdfs:label
  • De Kimpe aziridine synthesis (en)
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