http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-104420-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-33 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D407-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-647 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-26 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D407-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-04 |
| filingDate | 2016-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdd094cfe2f434202aace107ddf0eecb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b18aa29e050d3799734e3e668bffc241 |
| publicationDate | 2017-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-104420-A1 |
| titleOfInvention | BUTIROLACTONES AS HERBICIDES |
| abstract | In addition, compositions containing these compounds and methods for controlling unwanted vegetation are described; The methods comprise bringing the unwanted vegetation or its environment into contact with an effective amount of a compound or a composition of the present. Claim 1: A compound selected from formula (1), N-oxides and salts thereof, wherein Q¹ is a phenyl ring or a naphthalenyl ring system; each ring or ring system is optionally substituted with up to 5 substituents independently selected from R⁷; or a fully unsaturated 5- to 6-membered heteroaromatic ring or an 8 to 10-membered heteroaromatic bicyclic ring system; Each ring or ring system contains ring members selected from carbon atoms and from 1 to 4 heteroatoms independently selected from up to 2 O atoms, up to 2 S atoms and up to 4 N atoms, where up to 3 ring members that are carbon are independently selected from C (= O) and C (= S), and ring members that are sulfur atoms are independently selected from S (= O) ᵘ (= NR⁸) ᵛ; each ring or ring system is optionally substituted with up to 5 substituents independently selected from R⁷ in ring members that are carbon atoms and selected from R⁹ in ring members that are nitrogen atoms; Q² is a phenyl ring or a naphthalenyl ring system; each ring or ring system is optionally substituted with up to 5 substituents independently selected from R¹⁰; or a fully unsaturated 5- to 6-membered heteroaromatic ring or an 8 to 10-membered heteroaromatic bicyclic ring system; Each ring or ring system contains ring members selected from carbon atoms and from 1 to 4 heteroatoms independently selected from up to 2 O atoms, up to 2 S atoms and up to 4 N atoms, where up to 3 ring members that are carbon are independently selected from C (= O) and C (= S), and ring members that are sulfur atoms are independently selected from S (= O) ᵘ (= NR⁸) ᵛ; each ring or ring system is optionally substituted with up to 8 substituents independently selected from R¹⁰ in ring members that are carbon atoms and selected from R¹¹ in ring members that are nitrogen atoms; Y¹ and Y² are, independently, O, S or NR⁶; R¹ is H, hydroxy, amino, C₁₋₆ alkyl, C halo haloalkyl, C₂₋₆ alkenyl, C₃₋₆ alkynyl, C₂₋₈ alkoxyalkyl, C₂₋₈ haloalkoxyalkyl, C₂₋₈ alkylthioalkyl, Culf alkylsulphonylalkyl ₋₈, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₄₋₁₀ cycloalkylcarbonyl, C₂₋₈ alkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₂₋₈ alkylaminocarbonyl, C₃₋₁₀ dialkylaminocarbonyl, C₄₋₁₀ cycloalkylaminocarbonyl, C₁ alkoxy ₋₆, Cilt alkylthio, C₁₋₆ haloalkylthio, C₃₋₈ cycloalkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ haloalkylsulfinyl, C₃₋₈ cycloalkylsulfinyl, C₁₋₆ alkylsulfonyl, C₃₋₈ haloalkylsulfonyl, C₁ alkylsulfonyl, C₁ alkylaminosulfonyl ₋₆, Cquila dialkylaminosulfonyl, C₃₋₁₀ trialkylsilyl or G¹; R² and R³ are each independently H, halogen, hydroxy, C₁₋₄ alkyl, C₁₋₄ haloalkyl or C₁₋₄ alkoxy; or R² and R³ are taken together with the carbon atom to which they are attached to form a C₃₋₇ cycloalkyl ring; R⁴ and R⁵ are each, independently, H, halogen, hydroxyl, C₁₋₄ alkoxy or C₁₋₄ alkyl; each R⁶ is independently H, cyano, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ alkoxy, C₁₋₄ haloalkoxy, - (C = O) CH₃ or - (C = O) CF₃; each R⁸ is independently H, cyano, C₂₋₃ alkylcarbonyl or C₂₋₃ haloalkylcarbonyl; each R⁷ and R¹⁰ is independently halogen, cyano, nitro, C₁₋₈ alkyl, C₁₋₄ cyanoalkyl, C₁₋₄ cyanoalkoxy, C₁₋₈ haloalkyl, C₁₋₈ nitroalkyl, C₂₋₈ alkenyl, C₂₋₈ haloalkenyl, nitroalkenyl C₂₋₈, C₂₋₈ alkynyl, C₂₋₈ haloalkynyl, C₄₋₁₀ cycloalkylalkyl, C₄₋₁₀ halocycloalkylalkyl, C₅₋₁₂ alkylcycloalkylalkyl, C₅₋₁₂ cycloalkylalkyl, C₃₋₈ cycloalkylalkyl, C₃₋₈ alkylcycloalkyl, alkylcycloalkyl C₄₋₁₀, cycloalkylcycloalkyl C₆₋₁₂, cycloalkenyl C₃₋₈, halocycloalkenyl C₃₋₈, alkoxyalkyl C₂₋₈, haloalkoxyalkyl C₃₋₁₀, cycloalkoxyalkyl C₄₋₁₀, alkoxyalkoxyalkyl C₃₋₁₀, alkylthioalkyl C₂₋₈, alkylsulfinyl alkyl C₂₋₈, alkylsulfonylalkyl C₂₋₈, C₂₋₈ alkylaminoalkyl, C₂₋₈ haloalkylaminoalkyl, C₄₋₁ cycloalkylaminoalkyl ₀, Cquila dialkylaminoalkyl, -CHO, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, -C (= O) OH, C₂₋₈ alkoxycarbonyl, C₂₋₈ haloalkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₅ cycloalkylalkoxycarbonyl ₋₁₂, -C (= O) NH₂, C₂₋₈ alkylaminocarbonyl, C₄₋₁₀ cycloalkylaminocarbonyl, C₃₋₁₀ dialkylaminocarbonyl, C₁₋₈ haloalkoxy, C₂₋₈ alkoxyalkoxy, C₂₋₈ haloalkoxyalkoxy, C₂₋₈ alkenyloxy , C₂₋₈ haloalkenyloxy, C₃₋₈ alkynyloxy, C₃₋₈ haloalkyloxy, C₃₋₈ cycloalkoxy, C₃₋₈ halocycloalkoxy, C ciclo alkylcarbonylalkoxy, C₂₋₈ alkylcarbonyloxy, C₄₋₁₀ haloalkylcarbonyloxy, C₄₋₁₀ cycloalkylcarbonyloxy , C₁₋₈ alkylsulfonyloxy, C₁₋₈ haloalkylsulfonyloxy, C₁₋₈ alkylthio, C₁₋₈ haloalkylthio, C₃₋₈ cycloalkylthio alkyl Cs ilsulfinyl, C₁₋₈ haloalkylsulfinyl, C₁₋₈ alkylsulfonyl, C₁₋₈ haloalkylsulfonyl, C₃₋₈ cycloalkylsulfonyl, C₂₋₈ alkylcarbonylamino, C halo haloalkylcarbonylamino, C₁₋₆ alkylsulfonylamino, C₁₋₆ alkylsulfonylamino , -SF₅, -SCN, SO₂NH₂, Cqu trialkylsilyl, C₄₋₁₂ trialkylsilylalkyl, C₄₋₁₂ trialkylsilylalkoxy or G²; or two adjacent R⁷ are taken together with the carbon atoms to which they are attached to form a C₃₋₇ cycloalkyl ring; or two adjacent R¹⁰ are taken together with the carbon atoms to which they are attached to form a C₃₋₇ cycloalkyl ring; each R⁹ and R¹¹ is independently cyano, C₁₋₃ alkyl, C₂₋₃ alkenyl, C₂₋₃ alkynyl, C₃₋₆ cycloalkyl, C₁₋₃ alkoxyalkyl, C₂₋₃ alkylcarbonyl, C₂₋₃ alkoxycarbonyl, C₂ alkylaminoalkyl ₋₃ or Cquila dialkylaminoalkyl; each G¹ is, independently, phenyl, phenylmethyl, pyridinylmethyl, phenylcarbonyl, phenylcarbonyl (C alquilo alkyl), phenoxy, phenylethynyl, phenylsulfonyl or a 5- or 6-membered heteroaromatic ring, each optionally substituted on the ring members with up to 5 substituents independently selected from R¹²; each G² is, independently, phenyl, phenylmethyl, pyridinylmethyl, phenylcarbonyl, phenylcarbonyl (C₁₋₄ alkyl), phenoxy, phenylethynyl, phenylsulfonyl or a 5- or 6-membered heteroaromatic ring, each optionally substituted on the ring members with up to 5 substituents independently selected from R¹³; each R¹² and R¹³ is independently halogen, cyano, hydroxy, amino, nitro, -CHO, -C (= O) OH, -C (= O) NH₂, -SO₂NH₂, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₂ alkenyl ₋₆, C₂₋₆ alkynyl, C₂₋₈ alkylcarbonyl, C₂₋₈ haloalkylcarbonyl, C₂₋₈ alkoxycarbonyl, C₄₋₁₀ cycloalkoxycarbonyl, C₂₋₈ alkylaminocarbonyl, C₃₋₁₀ alkylaminocarbonyl, C₁₋ haloalkoxy ₆, C₂₋₈ alkylcarbonyloxy, C₁₋₆ alkylthio, C₁₋₆ haloalkylthio, C₁₋₈ alkylsulfinyl, C₁₋₆ haloalkylsulfinyl, C₁₋₆ alkylsulfonyl, C₁₋₆ haloalkylsulfonyl, C₂₋₈ alkylaminosulfonyl, C₃₋ dialkylaminosulfonyl, C₃₋ trialkylsilyl ₁₀, C₁₋₆ alkylamino, C₂₋₈ dialkylamino, C₂₋₈ alkylcarbonylamino, C₁₋₆ alkylsulfonylamino, phenyl, pyridinyl or thienyl; and each u and v is independently 0, 1 or 2 in each instance of S (= O) ᵘ (= NR⁸) ᵛ, provided that the sum of u and v is 0, 1 or 2. |
| priorityDate | 2015-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 51.