http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2549352-T3

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filingDate 2008-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_079e27c30e112b598d9185a1f7786a32
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publicationDate 2015-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2549352-T3
titleOfInvention Derivatives of tetramic acid and tetronic acid substituted with oxaespirocyclic spiro
abstract Compounds of formula (I), ** Formula ** in which W represents hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, substituted C3-C6 cycloalkyl, if necessary one to two times with C1 alkyl -C2, C1-C2 alkoxy, fluorine, chlorine, trifluoromethyl or C3-C6 cycloalkyl, halogen, C1-C6 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy or cyano, X represents halogen, C1-C6 alkyl, C2 alkenyl C6, C2-C6 alkynyl, C3-C6 cycloalkyl substituted in the case of one to two times with C1-C2 alkyl, C1-C2 alkoxy, fluorine, chlorine, trifluoromethyl or C3-C6 cycloalkyl, C1-C6 haloalkyl, C1- alkoxy C6, C3-C6-oxy alkenyl, C1-C6-thio alkyl, C1-C6-sulfinyl alkyl, C1-C6-sulfonyl alkyl, C1-C6 haloalkoxy, C3-C6-oxy haloalkenyl, nitro or cyano, Y and Z represent independently from each other hydrogen, halogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl substituted, where appropriate, one to two times with C1-C2 alkyl, C1-C2 alkoxy, fluorine, chlorine , trifluoromethyl or cycloalkyl or C3-C6, C1-C6 alkoxy, C1-C6 haloalkyl, C1-C6 haloalkoxy, cyano, C2-C6 alkenyl, C2-C6 alkynyl, or represents one of the (Het) -aryl moieties, ** Formula ** en where in the case of (Het) -aryl only one of the Y or Z moieties may represent (Het) -aryl, V1 represents hydrogen, halogen, C1-C12 alkyl, C1-C6 alkoxy, C1-C6-thio alkyl, alkyl C1-C6-sulfinyl, C1-C6 alkyl sulfonyl, C1-C4 haloalkyl, C1-C4 haloalkoxy, nitro, cyano or phenyl, phenoxy, phenoxy C1-C4 alkyl, phenyl C1-C4 alkoxy, phenylthioalkyl C1-C4 or Phenyl-C1-C4-thio-alkyl respectively substituted as appropriate once or several times with halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, nitro or cyano, V2 and V3 independently represent one of another hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 haloalkyl or C1-C4 haloalkoxy, A and B and the carbon atom (3 'or 4' position), to which they are attached represent a ring of tetrahydrofuran or a substituted tetrahydropyran ring given one to two times with C1-C6 alkyl, C1-C4 haloalkyl, C1-C6 alkoxy, or C1-C4 alkoxy-C1-C4 alkyl, D represents NH (1) or oxygen (2), Q1 and Q2 represent independently of each other hydrogen, C1-C6 alkyl, C1-C2 haloalkyl or C1-C4 alkoxy, G represents hydrogen (a) or represents one of the groups ** Formula ** in which E represents a metal ion or an ammonium ion , L represents oxygen or sulfur and M represents oxygen or sulfur, R1 represents C1-C20 alkyl, C2-C20 alkenyl, C1-C8 alkoxy-C1-C8 alkyl, C1-C8 alkyl-thio-C1-C8 alkyl or poly-alkoxy C1-C8-C1-C8 alkyl respectively substituted if necessary with halogen or cyano, or C3-C8 cycloalkyl substituted if necessary with halogen, C1-C6 alkyl or C1-C6 alkoxy, in which case one or two groups Non-directly adjacent methylene are replaced by oxygen and / or sulfur, phenyl substituted as appropriate with halogen, cyano, nitro, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, C1-C6 haloalkoxy, al C1-C6-thio or C1-C6-sulfonyl alkyl, phenyl-C1-C6 alkyl substituted as appropriate with halogen, nitro, cyano, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl or C1-C6 haloalkoxy , 5 or 6-membered heteroaryl with one or two heteroatoms of the substituted oxygen, sulfur and nitrogen group, if necessary with halogen or C1-C6 alkyl, phenoxy-C1-C6 alkyl substituted if necessary with halogen or C1-C6 alkyl or 5- or 6-membered heteroaryloxy-C1-C6 alkyl with one or two heteroatoms of the oxygen, sulfur and nitrogen group substituted where appropriate with halogen, amino or C1-C6 alkyl, R2 represents C1-C20 alkyl, C2-C20 alkenyl, C1-C8 alkoxy-C2-C8 alkyl or C1-C8 poly-alkoxy-C2-C8 alkyl respectively substituted where appropriate with halogen or cyano, C3-C8 cycloalkyl substituted if necessary with halogen, C1-C6 alkyl or C1- alkoxy C6 or phenyl or benzyl respectively substituted if necessary with halogen, cyano, nitro, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl or C1-C haloalkoxy 6, R3 represents substituted C1-C8 alkyl if necessary with halogen, or phenyl or benzyl respectively substituted if necessary with halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano or nitro , R4 and R5 independently represent each other C1-C8 alkyl, C1-C8 alkoxy, C1-C8-amino alkyl, di- (C1-C8 alkyl) amino, C1-C8-thio alkyl or C3-C8-thio alkenyl, respectively substituted if necessary with halogen, or phenyl, phenoxy or phenylthio respectively substituted if necessary with halogen, nitro, cyano, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4-thio alkyl, C1-C4-thio haloalkyl, C1-C4 alkyl or C1-C4 haloalkyl, R6 and R7 independently represent each other hydrogen, C1-C8 alkyl, C3-C8 cycloalkyl, C1-C8 alkoxy, C3-C8 alkenyl or C1-C8 alkoxy-C2-C8 alkyl respectively substituted if necessary with halogen or cyano, phenyl or benzyl respectively substituted if necessary with halogen, C1-C8 alkyl, C1-C8 haloalkyl or C1-C8 alkoxy, or together s represent a C3-C6 alkylene moiety substituted with C1-C6 alkyl, in which case a methylene group is replaced by oxygen or sulfur.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450067302
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7153
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID390985
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451318789
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393764
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID173820
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID689277
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393758
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416014093
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID689618
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID136037
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2724251
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393768
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID883175
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426086645
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393769
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID757355
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID52838
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID236421
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID197043
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16495729
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID226132
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1003
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID6248
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID764491
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID542820

Total number of triples: 869.