http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-4034295-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_da54f7ebbd2d9d8a82f92aca4d1b4e48 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-60 |
| filingDate | 1990-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c02b4614b24f3ce349803669b1dd1833 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0af56e82aa1f86b39e52ae690b21b19 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fc80a8eada01a13e300c01f2684abaa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_466226f0c9b6beb567a59388636c0659 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_97246e3cfe49623d8309a2d4578e9dac |
| publicationDate | 1992-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DE-4034295-A1 |
| titleOfInvention | SUBSTITUTED (BETA) -PYRIMIDINYLOXY (THIO) - AND (BETA) -TRIAZINYLOXY (THIO) CYCLOAL CANOL DERIVATIVES, METHODS FOR THE PRODUCTION THEREOF AND THEIR USE AS AGENTS WITH HERBICIDES, FUNGICIDES AND PLANTS |
| abstract | (A) Substd. beta-pyrimidinyloxy(thio) and beta-triazinyloxy(thio)cycloalkanol derivs. of formula (I) and their alkali metal salts, alkaline earth metal salts, ammonium salts or organic susbtd. ammonium salts and their optically active isomers are new. R1 = H, 1-4C alkyl, 1-4C alkoxyalkyl, benzyl (opt. susbtd. by 1-4C alkyl, halo(1-4C)alkyl, 1-4C alkoxy, halogen or NO2) or COR2, CO2R2 or SO2R2. R2 = 1-18C alkyl, halo (1-4C) alkyl, Ph or benzyl (these last 2 opt. substd. by 1-4C alkyl, halo (1-4C)alkyl, 1-4C alkoxy, halogen or NO2); R3 H, 1-10C alkyl, 2-10C alkenyl or 2-10C (these 3 opt. mono- or poly- substd. by opt. different 1-4C alkoxy, 1-4C alkylthio, amino, 1-4C alkylamino, di(1-4C)alkylamino, NO2, halogen or Ph gps), 3-8C cycloalkyl or 4-8C cycloalkenyl (these 2 opt. mono- or poly substd. by opt. different 1-4C alkyl, 1-4C alkoxy, 1-4C alkylthio, amino, 1-4C alkyl amino, di(1-4C)alkylamino, NO2, CF3, halogen or Ph gps.). or Ph; R5 and R6 - 1-4C alkyl, halo(1-4C) alkyl, 1-4C alkoxy, halo (1-4C) alkoxy, 1-4C alkoxy (1-4C)-alkyl, 1-4C alkylthio, 1-4C alkylamino, di(1-4C)-alkylamino or halogen; A = -(CR7R8)-; B = -(CR9R10)b-; D = -(CR11R12)d; E = -(CR13R14)e; F = -(CR15R16)f; G = -(CR17R18)g; R7-R18 = as described for R3 and R4; b, d, e, f and g = 0 or 1; X = O or S; Y = -CH= or -N=. (B) Intermediates of formula (II) are also new. Z = OV, where V = a suitable protecting gp. such as tert. butyldimethyl silyl or triphenylmethyl (IIa) or Z = a suitable leaving gp. such as halogen, alkylsulphonyloxy, haloalkylsulphonyloxy or phenylsulphonyloxy. USE/ADVANTAGE - (I) are selective herbicides effective against broad leaved weeds and grasses in various crops such as rape, soybeans, cotton, wheat, fruit trees, tea plants, etc. Suitable amts. for use are 0.001-5 kg/ha. (I) are also defoliants and desiccants and plant growth regulators. Some (I) are fungicides, (IIa) and (IIb) are intermediates in the prepn. of (I). |
| priorityDate | 1990-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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