ketimine - significado y definición. Qué es ketimine
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Qué (quién) es ketimine - definición


Ketimine Mannich reaction         
  • Scheme 11. BINOL phosphoric acid-catalyzed Mannich reaction of endocyclic N-acyl ketimines.
  • Scheme 12. Proline-catalyzed Mannich reaction of 3-substituted-2H-1,4-benzoxazines.
  • Scheme 13. Copper-catalyzed asymmetric Mannich reaction of 2H-azirines with β-ketoamides.
  • Scheme 14. Copper(I)-catalyzed asymmetric decarboxylative Mannich reaction of 2H-azirines.
  • Scheme 15. Zn-ProPhenol catalyzed asymmetric Mannich reaction of 2H-azirines with alkynyl cycloalkyl ketones.
  • Scheme 16. Chiral phosphoric acid-catalyzed Mukaiyama–Mannich reaction of endocyclic N-acyl ketimines.
  • Scheme 17. Copper-catalyzed Mannich reaction of N-unprotected isatin-derived ketimines.
  • Scheme 18. Stereodivergent asymmetric Mannich reaction of α-fluoronitriles with isatin-derived ketimines.
  • Scheme 20. Tandem α-alkenyl addition/proton shift reaction of silyl enol ethers with ketimines.
  • Scheme 21. Chiral organosuperbase-catalyzed direct Mannich reaction of ketiminoesters.
  • Scheme 22. Direct enantioselective Mannich reaction of α,β-unsaturated γ-butyrolactam with ketiminoesters.
  • Scheme 23. Direct catalytic Mannich reaction with an N-unprotected trifluoromethyl ketiminoester.
  • Scheme 24. Direct catalytic asymmetric vinylogous Mannich reaction of polyfluorinated alkynyl ketimines.
  • Scheme 25. Enantiodivergent Mannich reaction of alkynyl ketiminoesters catalyzed by chiral amines.
  • Scheme 26. Chiral amine-catalyzed Mannich reactions of (Z)-alkynyl alkyl ketimines.
CHEMICAL REACTION
Draft:Asymmetric Catalytic Ketimine Mannich Reactions
The ketimine Mannich reaction is an asymmetric synthetic technique using differences in starting material to push a Mannich reaction to create an enantiomeric product with steric and electronic effects, through the creation of a ketimine group. Typically, this is done with a reaction with proline or another nitrogen-containing heterocycle, which control chirality with that of the catalyst.
Imine         
  • Hexafluoroacetone imine is an unusual primary ketimine that is readily isolable.<ref name=OS/>
  • Imine synthesis from a primary amine and a carbonyl compound.
  •  Steps in pyridoxal phosphate-mediated reactions of [[alanine]] and [[cysteine]], illustrating one biological role for aldimines.
ANY CHEMICAL COMPOUND HAVING THE STRUCTURE RN=CR′R″, THUS ANALOGUE OF ALDEHYDE OR KETONE IN WHICH AN OXYGEN ATOM IS REPLACED BY SUBSTITUTED OR UNSUBSTITUTED NITROGEN ATOM
Aldimine; Imino; Imines; Ketimine; Acyl imidate; Aldimines; Ketimines; Imino group
In organic chemistry, an imine ( or ) is a functional group or organic compound containing a carbon–nitrogen double bond (). The nitrogen atom can be attached to a hydrogen or an organic group (R).
imine         
  • Hexafluoroacetone imine is an unusual primary ketimine that is readily isolable.<ref name=OS/>
  • Imine synthesis from a primary amine and a carbonyl compound.
  •  Steps in pyridoxal phosphate-mediated reactions of [[alanine]] and [[cysteine]], illustrating one biological role for aldimines.
ANY CHEMICAL COMPOUND HAVING THE STRUCTURE RN=CR′R″, THUS ANALOGUE OF ALDEHYDE OR KETONE IN WHICH AN OXYGEN ATOM IS REPLACED BY SUBSTITUTED OR UNSUBSTITUTED NITROGEN ATOM
Aldimine; Imino; Imines; Ketimine; Acyl imidate; Aldimines; Ketimines; Imino group
['?mi:n]
¦ noun Chemistry an organic compound containing the group ?C=NH or ?C=NR (where R is an alkyl group).
Origin
C19: from amine, on the pattern of the pair amide, imide.