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  • C07C45/00
    		•  Preparation of compounds having HB CC 4H006
  • C07C45/26
    		•  .by hydration of carbon-to-carbon triple bonds [3] HB CC 4H006
  • C07C45/27
    		•  .by oxidation [3] HB CC 4H006
  • C07C45/28
    		•  ..of —CHx-moieties [3] HB CC 4H006
  • C07C45/29
    		•  ..of hydroxy groups [3] HB CC 4H006
  • C07C45/30
    		•  ..with halogen containing compounds, e.g. hypohalogenation [3] HB CC 4H006
  • C07C45/31
    		•  ..with compounds containing mercury atoms, which may be regenerated in situ, e.g. by oxygen [3] HB CC 4H006
  • C07C45/32
    		•  ..with molecular oxygen [3] HB CC 4H006
  • C07C45/33
    		•  ...of CHx-moieties [3] HB CC 4H006
  • C07C45/34
    		•  ....in unsaturated compounds [3] HB CC 4H006
  • C07C45/35
    		•  .....in propene or isobutene [3] HB CC 4H006
  • C07C45/36
    		•  .....in compounds containing six-membered aromatic rings [3] HB CC 4H006
  • C07C45/37
    		•  ...of ∋C—O— functional groups to HB CC 4H006
  • C07C45/38
    		•  ....being a primary hydroxy group [3] HB CC 4H006
  • C07C45/39
    		•  ....being a secondary hydroxy group [3] HB CC 4H006
  • C07C45/40
    		•  .by oxidation with ozone; by ozonolysis [3] HB CC 4H006
  • C07C45/41
    		•  .by hydrogenolysis or reduction of carboxylic groups or functional derivatives thereof [3] HB CC 4H006
  • C07C45/42
    		•  .by hydrolysis [3] HB CC 4H006
  • C07C45/43
    		•  ..of 2 groups, X being halogen [3] HB CC 4H006
  • C07C45/44
    		•  .by reduction and hydrolysis of nitriles [3] HB CC 4H006
  • C07C45/45
    		•  .by condensation [3] HB CC 4H006
  • C07C45/46
    		•  ..Friedel-Crafts reactions [3] HB CC 4H006
  • C07C45/47
    		•  ..using phosgene [3] HB CC 4H006
  • C07C45/48
    		•  ..involving decarboxylation [3] HB CC 4H006
  • C07C45/49
    		•  .by reaction with carbon monoxide [3] HB CC 4H006
  • C07C45/50
    		•  ..by oxo-reactions [3] HB CC 4H006
  • C07C45/51
    		•  .by pyrolysis, rearrangement or decomposition [3] HB CC 4H006
  • C07C45/52
    		•  ..by dehydration and rearrangement involving two hydroxy groups in the same molecule [3] HB CC 4H006
  • C07C45/53
    		•  ..of hydroperoxides [3] HB CC 4H006
  • C07C45/54
    		•  ..of compounds containing doubly bound oxygen atoms, e.g. esters [3] HB CC 4H006
  • C07C45/55
    		•  ..of oligo- or polymeric oxo-compounds [3] HB CC 4H006
  • C07C45/56
    		•  .from heterocyclic compounds (C07C 45/55 takes precedence) [3] HB CC 4H006
  • C07C45/57
    		•  ..with oxygen as the only hetero atom [3] HB CC 4H006
  • C07C45/58
    		•  ...in three-membered rings [3] HB CC 4H006
  • C07C45/59
    		•  ...in five-membered rings (from ozonides C07C 45/40) [3] HB CC 4H006
  • C07C45/60
    		•  ...in six-membered rings [3] HB CC 4H006
  • C07C45/61
    		•  .by reactions not involving the formation of HB CC 4H006
  • C07C45/62
    		•  ..by hydrogenation of carbon-to-carbon double or triple bonds [3] HB CC 4H006
  • C07C45/63
    		•  ..by introduction of halogen; by substitution of halogen atoms by other halogen atoms [3] HB CC 4H006
  • C07C45/64
    		•  ..by introduction of functional groups containing oxygen only in singly bound form [3] HB CC 4H006
  • C07C45/65
    		•  ..by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups [3] HB CC 4H006
  • C07C45/66
    		•  ...by dehydration [3] HB CC 4H006
  • C07C45/67
    		•  ..by isomerisation; by change of size of the carbon skeleton [3] HB CC 4H006
  • C07C45/68
    		•  ...by increase in the number of carbon atoms [3] HB CC 4H006
  • C07C45/69
    		•  ....by addition to carbon-to-carbon double or triple bonds [3] HB CC 4H006
  • C07C45/70
    		•  ....by reaction with functional groups containing oxygen only in singly bound form [3] HB CC 4H006
  • C07C45/71
    		•  .....being hydroxy groups [3] HB CC 4H006
  • C07C45/72
    		•  ....by reaction of compounds containing HB CC 4H006
  • C07C45/73
    		•  .....combined with hydrogenation [3] HB CC 4H006
  • C07C45/74
    		•  .....combined with dehydration [3] HB CC 4H006
  • C07C45/75
    		•  .....Reactions with formaldehyde [3] HB CC 4H006
  • C07C45/76
    		•  ...with the aid of ketenes [3] HB CC 4H006
  • C07C45/77
    		•  .Preparation of chelates of aldehydes or ketones [3] HB CC 4H006
  • C07C45/78
    		•  .Separation; Purification; Stabilisation; Use of additives [3] HB CC 4H006
  • C07C45/79
    		•  ..by solid-liquid treatment; by chemisorption [3] HB CC 4H006
  • C07C45/80
    		•  ..by liquid-liquid treatment [3] HB CC 4H006
  • C07C45/81
    		•  ..by change in the physical state, e.g. crystallisation [3] HB CC 4H006
  • C07C45/82
    		•  ...by distillation [3] HB CC 4H006
  • C07C45/83
    		•  ....by extractive distillation [3] HB CC 4H006
  • C07C45/84
    		•  ....by azeotropic distillation [3] HB CC 4H006
  • C07C45/85
    		•  ..by treatment giving rise to a chemical modification [3] HB CC 4H006
  • C07C45/86
    		•  ..Use of additives, e.g. for stabilisation [3] HB CC 4H006
  • C07C45/87
    		•  .Preparation of ketenes or dimeric ketenes [3] HB CC 4H006
  • C07C45/88
    		•  ..from ketones [3] HB CC 4H006
  • C07C45/89
    		•  ..from carboxylic acids, their anhydrides, esters or halides [3] HB CC 4H006
  • C07C45/90
    		•  ..Separation; Purification; Stabilisation; Use of additives [3] HB CC 4H006
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