http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0304920-A2

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filingDate 1988-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41a5837ccb39cc05aef60644e558f3c4
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publicationDate 1989-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0304920-A2
titleOfInvention Condensed heterocyclic derivatives, process for their production and herbicides
abstract A condensed heterocyclic derivative having the formula:n wherein X is an oxygen atom or a sulfur atom: and Z isn wherein G is a hydrogen atom or a halogen atom; A is a halogen atom or NO2; E is a hydrogen atom, a halogen atom, C≡N, NO 2 , NH 2 , OH, SH, OR 1 (wherein R, is C 1 -C 5 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl, C 2 -C 4 alkenyl, C 3 -C 4 alkynyl,n wherein each of Qa and Qb is an oxygen atom or a sulfur atom, R 1a is a hydrogen atom or C 1 -C 3 alkyl, R 1b is a hydrogen atom, C 1 -C 5 alkyl, C 2 -C 5 alkenyl, C 3 -C 5 alkynyl. C 2 -C 3 haloalkyl, C 1 -C 2 alkoxy (C 1 -C 2 ) alkyl, C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl, C 3 -C 6 cycloalkyl, CH 2 CO 2 -(C 1 -C 3 alkyl) or CH(CH 3 )-CO 2 -(C 1 -C 2 alkyl), or R 1a and R 1b together form an alkylene group which in turn forms, together withn -Qb-, a 4-6 memberd lactone ring,n wherein R 1a and Qa are as defined above, each of R 1c and R id is a hydrogen atom, C 1 -C 5 alkyl, C 2 -C 5 alkenyl, C 3 -C 5 alkynyl, C 2 -C 5 haloalkyl, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl, or R 1d and R 1c together form an alkylene group which in turn forms, together with the adjacent nitrogen atom, a 5-7 membered ring, CH 2 C≡N, tetrahydropyranyl, tetrahydrothiopyranyl, CH 2 COR 1e ,n wherein R 1e is C 1 -C 3 alkyl, R 1f is a hydrogen atom, C 1 -C 3 alkyl, CH 2 CO 2 -(C 1 -C 3 alkyl) or COCHs, or C 1 -C 2 alkoxy (C 1 -C 2 ) alkyl), SR 3 (wherein R 3 has the same meaning as R 1 defined above), CO 2 R 5 (wherein Rs is a hydrogen atom, C 1 -C 5 alkyl, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl), NHR 6 (wherein R 6 is C 1 -Cs alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl, C 2 -C 4 . alkenyl or C 3 -C 4 alkynyl), or CH=NOR 7 -(wherein R 7 is a hydrogen atom, C 1 -C 5 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl, C 2 -C 4 alkenyl or C 3 -C 4 . alkynyl); L is a hydrogen atom or a halogen atom; Y is an oxygen atom or a sulfur atom; n is an integer of 0 or 1; J is a hydrogen atom, a halogen atom, Ci-Cs alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl, C 2 -C 4 . alkenyl, C 3 -C 4 alkynyl, C 1 -C 5 haloalkyl, C 3 -C 4 haloalkenyl, C 3 -C 4 haloalkynyl, C 1 -C 2 alkoxy (C 1 -C 2 ) alkyl, CH 2 C≡N, CH 2 CO 2 R 8 (wherein Rs is a hydrogen atom, C 1 -C 5 alkyl, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl) or CH 2 CH 2 CO 2 R 9 (wherein R 9 is a hydrogen atom, C 1 -C 5 alkyl, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkyl (C 1 -C 2 ) alkyl).
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88513127
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127559277
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234903746
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19931749
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426284782
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4121
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234076899
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415728482
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4499
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420420645
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226441308
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234094080
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226411549
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129821549
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4499

Total number of triples: 593.