FI (list display)

  • C07D505/00
  • Heterocyclic compounds containing 5-oxa-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula: , e.g. oxacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with a HB CC 4C072
  • C07D505/02
  • .Preparation(by microbiological processes C12P17/18) [6] HB CC 4C072
  • C07D505/04
  • ..by forming the ring or condensed ring systems [6] HB CC 4C072
  • C07D505/06
  • ..maufacturing where starting compounds are compounds already containing the ring or condensed ring systems, e.g. by dehydrogenation of the ring, by introduction, elimination or modification of substituents [6] HB CC 4C072
  • C07D505/08
  • ...Modification of a carboxyl group directly attached in position 2, e.g. esterification [6] HB CC 4C072
  • C07D505/10
  • .with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 [6] HB CC 4C072
  • C07D505/12
  • ..substituted in position 7 [6] HB CC 4C072
  • C07D505/14
  • ...with hetero atoms directly attached in position 7 [6] HB CC 4C072
  • C07D505/16
  • ....Nitrogen atoms [6] HB CC 4C072
  • C07D505/18
  • .....further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof [6] HB CC 4C072
  • C07D505/20
  • ......with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen [6] HB CC 4C072
  • C07D505/22
  • .......further substituted by singly-bound nitrogen atoms [6] HB CC 4C072
  • C07D505/24
  • .......further substituted by doubly-bound nitrogen atoms [6] HB CC 4C072
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