http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-20002089-A3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_36089addd8e49e968b4c7e13c517dd1c |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-48 |
| filingDate | 1998-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f41531ec52d82552781e3c7742cc9c69 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_caf85445449ce64cf6e527ea80bd8019 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0290f8648e3074d507bb4b44e0095f06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc3a347e4d826fa30c89b199ad15b6e7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f40ca240ab5fd77b179f9fde6bc73c9 |
| publicationDate | 2000-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CZ-20002089-A3 |
| titleOfInvention | Diol compounds |
| abstract | The diol compounds of formula II wherein R 1 is chloro, fluoronor trifluoromethyl, R 2 is hydrogen, chloro, fluoro orntrifluoromethyl; and R is a hydrogen atom or a protecting groupnhydroxyl groups useful as an intermediate for synthesisnantimycotic azole compounds. One of the describednThe methods for producing compounds II are based on iodine or iodinenbromobenzene derivatives. Corresponding Grignard reagentnis converted to the phenylzinc halide or phenylboronic acidnfollowed by hydrolysis with iodine or bromofuramate vnthe presence of a suitable transition catalystnmetal. The diester thus obtained is reduced by known methods tonCompound II. |
| priorityDate | 1998-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 95.