FI (list display)

  • C07C209/00
  • Preparation of compounds containing amino groups bound to a carbon skeleton [5] HB CC 4H006
  • C07C209/02
  • .by substitution of hydrogen atoms by amino groups [5] HB CC 4H006
  • C07C209/04
  • .by substitution of functional groups by amino groups [5] HB CC 4H006
  • C07C209/06
  • ..by substitution of halogen atoms [5] HB CC 4H006
  • C07C209/08
  • ...with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings [5] HB CC 4H006
  • C07C209/10
  • ...with formation of amino groups bound to carbon atoms of six-membered aromatic rings or from amines having nitrogen atoms bound to carbon atoms of six-membered aromatic rings [5] HB CC 4H006
  • C07C209/12
  • ...with formation of quaternary ammonium compounds [5] HB CC 4H006
  • C07C209/14
  • ..by substitution of hydroxy groups or of etherified or esterified hydroxy groups [5] HB CC 4H006
  • C07C209/16
  • ...with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings [5] HB CC 4H006
  • C07C209/18
  • ...with formation of amino groups bound to carbon atoms of six-membered aromatic rings or from amines having nitrogen atoms bound to carbon atoms of six-membered aromatic rings [5] HB CC 4H006
  • C07C209/20
  • ...with formation of quaternary ammonium compounds [5] HB CC 4H006
  • C07C209/22
  • ..by substitution of other functional groups [5] HB CC 4H006
  • C07C209/24
  • .by reductive alkylation of ammonia, amines or compounds having groups reducible to amino groups, with carbonyl compounds [5] HB CC 4H006
  • C07C209/26
  • ..by reduction with hydrogen [5] HB CC 4H006
  • C07C209/28
  • ..by reduction with other reducing agents [5] HB CC 4H006
  • C07C209/30
  • .by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds [5] HB CC 4H006
  • C07C209/32
  • ..by reduction of nitro groups [5] HB CC 4H006
  • C07C209/34
  • ...by reduction of nitro groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings [5] HB CC 4H006
  • C07C209/36
  • ...by reduction of nitro groups bound to carbon atoms of six-membered aromatic rings [5] HB CC 4H006
  • C07C209/38
  • ..by reduction of nitroso groups [5] HB CC 4H006
  • C07C209/40
  • ..by reduction of hydroxylamino or oxyimino groups [5] HB CC 4H006
  • C07C209/42
  • ..by reduction of nitrogen-to-nitrogen bonds [5] HB CC 4H006
  • C07C209/44
  • .by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers [5] HB CC 4H006
  • C07C209/46
  • ..by reduction of carboxylic acids or esters thereof in presence of ammonia or amines [5] HB CC 4H006
  • C07C209/48
  • ..by reduction of nitriles [5] HB CC 4H006
  • C07C209/50
  • ..by reduction of carboxylic acid amides [5] HB CC 4H006
  • C07C209/52
  • ..by reduction of imines or imino-ethers (C07C 209/24 takes precedence) [5] HB CC 4H006
  • C07C209/54
  • .by rearrangement reactions [5] HB CC 4H006
  • C07C209/56
  • ..from carboxylic acids involving a Hofmann, Curtius, Schmidt, or Lossen-type rearrangement [5] HB CC 4H006
  • C07C209/58
  • ..from or via amides [5] HB CC 4H006
  • C07C209/60
  • .by condensation or addition reactions, e.g. Mannich reaction, addition of ammonia or amines to alkenes or to alkynes or addition of compounds containing an active hydrogen atom to Schiff's bases, quinone imines, or aziranes [5] HB CC 4H006
  • C07C209/62
  • .by cleaving carbon-to-nitrogen, sulfur-to-nitrogen, or phosphorus-to-nitrogen bonds, e.g. hydrolysis of amides, N-dealkylation of amines or quaternary ammonium compounds (C07C 209/24 takes precedence) [5] HB CC 4H006
  • C07C209/64
  • .by disproportionation [5] HB CC 4H006
  • C07C209/66
  • .from or via metallo-organic compounds [5] HB CC 4H006
  • C07C209/68
  • .from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton [5] HB CC 4H006
  • C07C209/70
  • ..by reduction of unsaturated amines [5] HB CC 4H006
  • C07C209/72
  • ...by reduction of six-membered aromatic rings [5] HB CC 4H006
  • C07C209/74
  • ..by halogenation, hydrohalogenation, dehalogenation, or dehydrohalogenation [5] HB CC 4H006
  • C07C209/76
  • ..by nitration [5] HB CC 4H006
  • C07C209/78
  • ..from carbonyl compounds, e.g. from formaldehyde, and amines having amino groups bound to carbon atoms of six-membered aromatic rings, with formation of methylene-diarylamines [5] HB CC 4H006
  • C07C209/80
  • .by photochemical reactions; by using free radicals [5] HB CC 4H006
  • C07C209/82
  • .Purification; Separation; Stabilisation; Use of additives [5] HB CC 4H006
  • C07C209/84
  • ..Purification [5] HB CC 4H006
  • C07C209/86
  • ..Separation [5] HB CC 4H006
  • C07C209/88
  • ...Separation of optical isomers [5] HB CC 4H006
  • C07C209/90
  • ..Stabilisation; Use of additives [5] HB CC 4H006
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