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1. 发明申请

WO1996006071A1 NOVEL HERBICIDAL CYCLOHEXANE-1,3-DIONE DERIVATIVES AND THEIR PREPARATION PROCESS 审中-公开
标题翻译：新型除草剂环己烷-1,3-二酮衍生物及其制备方法
公开(公告)号：WO1996006071A1
公开(公告)日：1996-02-29
申请号：PCT/KR1995000092
申请日：1995-07-24
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , RYU, Eung, Kul , KIM, Kyoung, Mahn , KIM, Jae, Nyoung , KIM, Jin, Seog
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07C251/42
CPC分类号： C07C251/66 , A01N35/10 , C07C17/35 , C07C45/455 , C07C45/46 , C07C45/513 , C07C45/74 , C07C251/42 , C07C251/52 , C07C251/54 , C07C2601/16 , C07C2602/08 , C07C25/22 , C07C49/657 , C07C49/697 , C07C49/67 , C07C49/683 , C07C47/546 , C07C47/55 , C07C49/237 , C07C49/225
摘要： The present invention relates to novel cyclohexane-1,3-dione derivatives of formula (1) useful as herbicides and plant-growth regulants, wherein X is selected from the group consisting of hydrogen, halogen, C1-C6 alkyl, C2-C6 alkoxy, C1-C6 haloalkyl, nitro, C1-C6 alkylthio, C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C1-C6 sulfamoyl, and N, N-di(C1-C6 alkyl)sulfamoyl group; (X)n represents the number of X substituents which may be substituted on benzene ring, wherein n is 1, 2 or 3. Also, cyclohexyl moiety, one of the substituents on benzofuran ring, is substituted at C-4, C-5, C-6 or C-7 position on benzene ring; R is selected from the group consisting of hydrogen and C1-C6 alkyl group; R is selected from the group consisting of C1-C6 alkyl, C2-C6 alkenyl and C2-C6 alkynyl group; R is selected from the group consisting of hydrogen, C1-C6 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkoxyalkyl, C2-C6 alkylthioalkyl, benzyl and C2-C6 haloalkanoyl group; R is selected from the group consisting of hydrogen, alkali metal cation, alkaline earth metal cation, C1-C4 alkanoyl, C1-C4 haloalkanoyl and benzoyl group.
摘要翻译：本发明涉及用作除草剂和植物生长调节剂的式（1）的新型环己烷-1,3-二酮衍生物，其中X选自氢，卤素，C 1 -C 6烷基，C 2 -C 6烷氧基，C 1 -C 6卤代烷基，硝基，C 1 -C 6烷硫基，C 1 -C 6烷基亚磺酰基，C 1 -C 6烷基磺酰基，C 1 -C 6氨磺酰基和N，N-二（C 1 -C 6烷基）氨磺酰基; （X）n表示可在苯环上取代的X取代基的数目，其中n为1,2或3.此外，苯并呋喃环上的取代基之一的环己基部分在C-4，C-5 ，苯环上的C-6或C-7位; R 1选自氢和C 1 -C 6烷基; R 2选自C 1 -C 6烷基，C 2 -C 6烯基和C 2 -C 6炔基; R 3选自氢，C 1 -C 6烷基，C 1 -C 6卤代烷基，C 2 -C 6烯基，C 2 -C 6卤代烯基，C 2 -C 6烷氧基烷基，C 2 -C 6烷硫基烷基，苄基和C 2 -C 6卤代烷酰基 ; R 4选自氢，碱金属阳离子，碱土金属阳离子，C1-C4烷酰基，C1-C4卤代烷酰基和苯甲酰基。

2. 发明申请

WO1994003443A1 HERBICIDAL CYCLOHEXANE-1,3-DIONE DERIVATIVES AND THEIR PREPARATION PROCESS 审中-公开
标题翻译：除草环己烷-1,3-二酮衍生物及其制备方法
公开(公告)号：WO1994003443A1
公开(公告)日：1994-02-17
申请号：PCT/KR1993000069
申请日：1993-08-06
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , RYU, Eung, Kul , KIM, Kyoung, Mahn , KIM, Hyoung, Rae , SONG, Jong, Hwan , KIM, Jae, Nyoung , KIM, Jin, Seog
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D307/81
CPC分类号： C07D307/79 , A01N43/12
摘要： The present invention relates to novel cyclohexane-1,3-dione derivatives of formula (I) useful as herbicides and plant-growth regulants, wherein, X is selected from the group consisting of hydrogen, C1-C6 alkyl, C2-C6 alkoxy, halogen, C1-C6 haloalkyl, nitro, cyano, C1-C6 alkylthio, C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, sulfamoyl, N-(C1-C6 alkyl)sulfamoyl and N,N-di(C1-C6 alkyl)sulfamoyl group; (X)n represents number of X substituents which may be the same or different on benzene ring, where n is 1, 2 or 3. Also, cyclohexyl moiety, one of the substituents on benzofuran ring, is substituted at 4, 5, 6 or 7 position. The (X)n cannot be filled only with hydrogens and the (X)n can substitute position where cyclohexyl moiety is not substituted; R1 is selected from hydrogen and C1-C4 alkyl group; R2 is selected from C1-C6 alkyl, C2-C6 alkenyl and C2-C6 alkynyl group; R3 is selected from hydrogen, C1-C6 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkoxyalkyl, C2-C6 alkylthioalkyl, benzyl and C2-C6 haloalkanoyl group; R4 is selected from hydrogen, alkali metal cation, alkaline earth metal cation, C1-C4 alkanoyl, C1-C4 haloalkanoyl and benzoyl group.
摘要翻译：本发明涉及可用作除草剂和植物生长调节剂的式（I）的新型环己烷-1,3-二酮衍生物，其中X选自氢，C 1 -C 6烷基，C 2 -C 6烷氧基，卤素，C 1 -C 6卤代烷基，硝基，氰基，C 1 -C 6烷硫基，C 1 -C 6烷基亚磺酰基，C 1 -C 6烷基磺酰基，氨磺酰基，N-（C 1 -C 6烷基）氨磺酰基和N，N-二（C 1 -C 6烷基）组; （X）n表示在苯环上可以相同或不同的X取代基的数目，其中n为1,2或3.此外，苯并呋喃环上的取代基之一的环己基部分在4,5,6 或7位。（X）n不能仅用氢气填充，（X）n可以替代环己基部分未被取代的位置; R1选自氢和C1-C4烷基; R2选自C1-C6烷基，C2-C6烯基和C2-C6炔基; R 3选自氢，C 1 -C 6烷基，C 1 -C 6卤代烷基，C 2 -C 6烯基，C 2 -C 6卤代烯基，C 2 -C 6烷氧基烷基，C 2 -C 6烷硫基烷基，苄基和C 2 -C 6卤代烷酰基; R4选自氢，碱金属阳离子，碱土金属阳离子，C1-C4烷酰基，C1-C4卤代烷酰基和苯甲酰基。

3. 发明申请

WO1997047615A1 PROCESS FOR PREPARING 2,3-DIHYDRO-2-METHYL-2-ALKYLBENZOFURAN DERIVATIVES 审中-公开
标题翻译：制备2,3-二羟基-2-甲基-2-烷基苯并呋喃衍生物的方法
公开(公告)号：WO1997047615A1
公开(公告)日：1997-12-18
申请号：PCT/KR1996000090
申请日：1996-06-12
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , RYU, Eung, Kul , KIM, Kyoung, Mahn
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D307/79
CPC分类号： C07D307/79
摘要： The present invention relates to process for preparing 2,3-dihydro-2-methyl-2-alkylbenzofuran derivatives of formula (I) useful as intermediate of agricultural chemicals and pharmaceutical products, wherein X is selected from the group consisting of hydrogen, halogen, hydroxy group, aldehyde group and C1-C6 alkyl group; and R is selected from the group consisting of C1-C6 alkyl group.
摘要翻译：本发明涉及制备式（I）的2,3-二氢-2-甲基-2-烷基苯并呋喃衍生物的方法，其用作农药和药物的中间体，其中X选自氢，卤素，羟基，醛基和C 1 -C 6烷基; 并且R选自C 1 -C 6烷基。

4. 发明申请

WO1994004530A1 HERBICIDAL QUINOLINYLOXADIAZOLES 审中-公开
标题翻译：除草剂喹喔啉二恶唑
公开(公告)号：WO1994004530A1
公开(公告)日：1994-03-03
申请号：PCT/KR1993000073
申请日：1993-08-13
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , RYU, Eung, Kul , CHUNG, Kun, Hoe , LEE, Won, Hee , KIM, Jae, Nyoung , HONG, Kyung, Sik
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D413/04
CPC分类号： C07D413/04 , A01N43/82
摘要： The present invention relates to novel quinolinyloxadiazole derivatives of formula (I) having processes for their preparation and their use as herbicides and plant growth regulants, especially their use in the selective kill and control of barnyardgrass in the presence of rice. Formula (I), wherein A and B are selected from the group consisting of hydrogen, halogen and C1-C3 lower alkyl; R is a C3-C4 alkyl or cycloalkyl, phenyl, pyridyl, benzyl, phenoxyalkyl or phenylthioalkyl, and aromatic groups in these radicals are optionally substituted with 1 -- 3 substituents selected from the group consisting of halogen, C1-C4 alkyl C1-C4 alkoxy, C1-C4 alkylthio, C2-C6 alkoxyalkyl and an anolog thereof.
摘要翻译：本发明涉及式（I）的新型喹啉喔啉二唑衍生物，其具有制备方法及其作为除草剂和植物生长调节剂的用途，特别是其在水稻存在下选择性杀死和控制稗草的用途。式（I），其中A和B选自氢，卤素和C 1 -C 3低级烷基; R是C 3 -C 4烷基或环烷基，苯基，吡啶基，苄基，苯氧基烷基或苯硫基烷基，这些基团中的芳族基团任选地被1-3个选自以下的取代基取代：卤素，C 1 -C 4烷基C 1 -C 4 烷氧基，C 1 -C 4烷硫基，C 2 -C 6烷氧基烷基及其阴离子。

5. 发明申请

WO1992015568A1 BENZENESULFONYLUREA DERIVATIVES 审中-公开
标题翻译：苯并呋喃衍生物
公开(公告)号：WO1992015568A1
公开(公告)日：1992-09-17
申请号：PCT/KR1992000007
申请日：1992-03-09
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , KIM, Dae-Whang , KO, Young, Kwan , KIM, Jin-Seog , KU, Dong, Whan
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D239/42
CPC分类号： C07D521/00 , A01N47/36 , C07C311/29
摘要： The present invention relates to novel benzenesulfonylurea derivatives, having a herbicidal activity, which is described in the structure of general formula (I), wherein R is H, C1-C3 alkyl, C1-C3 haloalkyl, halogen, CN, NO2, C1-C3 alkoxy, C1-C3 haloalkoxy, SO2NR R , C1-C3 alkylthio, C1-C3 alkylsulfinyl, C1-C3 alkylsulfonyl, SCH2F, NH2, NHCH3, N(Me)2, C1-C2 alkyl substituted with C1-C2 alkoxy, C1-C2 haloalkoxy, SH, SCH3, CN or OH, or CO2R ; and then R is H, C1-C4 alkyl, C2-C3 cyanoalkyl, methoxy or ethoxy; R is H, C1-C4 alkyl, C3-C4 alkenyl, or when taken together connecting R and R , -(CH2)3-, -(CH2)4-, -(CH2)5- or CH2CH2OCH2CH2-, may be formed; R is C1-C4 alkyl, C3-C4 alkenyl, C3-C4 alkynyl, C1-C4 alkyl substituted with 1 SIMILAR 3 halogens or cyano groups, C5-C6 cycloalkyl, C3-C7 cycloalkylalkyl or C2-C4 alkoxyalkyl; R is C1-C6 alkyl substituted with 1 SIMILAR 3 halogens; R is H or CH3; W is O or S; A is a heterocyclic ring defined in the specification; and these may be an agriculturally suitable salt.
摘要翻译：本发明涉及具有除草活性的新型苯磺酰脲衍生物，其在通式（I）的结构中描述，其中R 1是H，C 1 -C 3烷基，C 1 -C 3卤代烷基，卤素，CN，NO 2 ，C 1 -C 3烷氧基，C 1 -C 3卤代烷氧基，SO 2 NR R 1，C 1 -C 3烷硫基，C 1 -C 3烷基亚磺酰基，C 1 -C 3烷基磺酰基，SCH 2 F，NH 2，NHCH 3，N（Me）被C 1 -C 2烷氧基，C 1 -C 2卤代烷氧基，SH，SCH 3，CN或OH或CO 2 R III取代的烷基; 然后R 1是H，C 1 -C 4烷基，C 2 -C 3氰基烷基，甲氧基或乙氧基; 或者当R 1和R 2连接在一起时， - （CH 2）3 - ， - （CH 2）4 - ， - （CH 2） 5-或CH 2 CH 2 OCH 2 CH 2 - 可以形成; R III是C 1 -C 4烷基，C 3 -C 4烯基，C 3 -C 4炔基，被1个3个卤素或氰基取代的C 1 -C 4烷基，C 5 -C 6环烷基，C 3 -C 7环烷基烷基或C 2 -C 4烷氧基烷基; R 2是被1个3个卤素取代的C 1 -C 6烷基; R 3是H或CH 3; W为O或S; A是说明书中定义的杂环; 这些可以是农业上合适的盐。

6. 发明申请

WO1996012708A1 HERBICIDAL SULFONYL UREA DERIVATIVES 审中-公开
标题翻译：除草剂磺酰脲衍生物
公开(公告)号：WO1996012708A1
公开(公告)日：1996-05-02
申请号：PCT/KR1994000147
申请日：1994-10-24
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , KIM, Dae, Whang , KO, Young, Kwan , CHANG, Hae, Sung , RYU, Jae, Wook , JO, In, Ho , WOO, Jae, Chun , KU, Dong, Whan , KIM, Jin, Seog
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D239/42
CPC分类号： C07D521/00 , A01N47/36 , C07C311/29
摘要： The present invention relates to novel sulfonyl urea derivatives of formula (I) having erythro-type stereoisomer as herbicides for treatment of pre-emergence and/or post-emergence, their use and composition as agriculturally suitable herbicides, wherein, P and Q, as equivalent or different group respectively, are CH or N, and present as aromatic ring including P and Q as benzene or pyridine ring; R is H, (a) or (b) group, wherein R is C1 SIMILAR C4 alkyl, C1 SIMILAR C3 haloalkyl, C2 SIMILAR C4 alkenyl or C2 SIMILAR C4 alkynyl group, wherein X is O, S, NH or NR group; R' is H or CH3 group; and X and Y are independently halogen atom, C1 SIMILAR C2 alkyl, C1 SIMILAR C2 alkoxy or C1 SIMILAR C2 haloalkoxy group.
摘要翻译：本发明涉及式（I）的新型磺酰脲衍生物，其具有用作治疗出苗前和/或出苗后的除草剂的红血型立体异构体，其用途和组合物作为农业上合适的除草剂，其中P和Q为分别为CH或N，作为芳香环，包括P和Q作为苯或吡啶环; R是H，（a）或（b）基团，其中R a是C 1 -C 4 C4烷基，C 1 -C 3卤代烷基，C 2 C 4烯基或C 2 C 4 C 4炔基，其中X a是O，S， NH或NR a基团; R'是H或CH 3基团; 且X和Y独立地为卤素原子，C1-C2烷基，C1-C2烷氧基或C1-C2 C2卤代烷氧基。

7. 发明申请

WO1998002444A1 PROCESS FOR THE PREPARATION OF DIALKYLALUMINUM ALKOXIDE 审中-公开
标题翻译：制备烷基氧化铝的方法
公开(公告)号：WO1998002444A1
公开(公告)日：1998-01-22
申请号：PCT/KR1997000102
申请日：1997-06-04
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , KIM, Yunsoo , KOH, Wonyong
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07F05/06
CPC分类号： C07F5/066
摘要： Dialkylaluminum alkoxide represented by R 2AlOR wherein R and R are each independently a C1-10 alkyl group, is economically prepared by reacting a trialkylaluminum with an aluminum alkoxide at or near ambient temperature.
摘要翻译：由R 1，2AlOR 2表示的二烷基铝醇盐，其中R 1和R 2各自独立地为C 1-10烷基，经济地通过在室温或接近环境温度下使三烷基铝与烷氧基铝反应制备。

8. 发明申请

WO1997005088A1 PROCESS FOR PREPARING HYDROCARBONS 审中-公开
标题翻译：制备油料的方法
公开(公告)号：WO1997005088A1
公开(公告)日：1997-02-13
申请号：PCT/KR1995000139
申请日：1995-10-27
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , LEE, Kyu-Wan , CHOI, Myuong-Jae , JUN, Ki-Won , CHOI, Pyoung, Ho , LEE, Soo-Jae
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07C01/12
CPC分类号： B01J23/78 , C07C1/12 , C07C2521/04 , C07C2523/04 , C07C2523/745 , C07C2523/78
摘要： This invention relates to a process for preparing hydrocarbons, in particular hydrogenation of carbon dioxide over Fe-K/Al2O3 catalyst, which is reduced in hydrogen and activated in the mixture of carbon dioxide and hydrogen.
摘要翻译：本发明涉及一种制备烃的方法，特别是在Fe-K / Al 2 O 3催化剂上二氧化碳的氢化，其在氢中还原并在二氧化碳和氢气的混合物中活化。

9. 发明申请

WO1996025923A1 A PROCESS FOR THE PREPARATION OF AN EMULSION NETWORK FOR A TRANSDERMAL DRUG DELIVERY SYSTEM 审中-公开
标题翻译：用于制备用于传送药物递送系统的乳化网络的方法
公开(公告)号：WO1996025923A1
公开(公告)日：1996-08-29
申请号：PCT/KR1996000026
申请日：1996-02-22
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , YUK, Soonhong , CHO, Sunhang , LEE, Haibang
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： A61K09/70
CPC分类号： A61K9/7023 , A61K9/06 , A61K9/107
摘要： A process for the preparation of an emulsion network for a transdermal drug delivery system comprising the steps of mixing a polymer (or monomer) aqueous solution with oil using a homogenizer to produce an emulsion solution, adding drugs and additives to the emulsion solution, solidifying the emulsion solution by the process of adding metal ions, cooling, irradiating ultra violet rays based on the polymer used and shaping the solidified emulsion solution applicable to the use thereof.
摘要翻译：一种用于制备透皮药物递送系统的乳液网络的方法，包括以下步骤：使用均化器将聚合物（或单体）水溶液与油混合以产生乳液，向乳液中加入药物和添加剂，通过添加金属离子的过程，冷却，基于所使用的聚合物照射紫外线并成形适用于其使用的固化乳液的乳液。

10. 发明申请

WO1996006675A1 PHOTOCATALYST, METHOD FOR PREPARING THE SAME, AND PRODUCTION OF HYDROGEN USING THE SAME 审中-公开
标题翻译：光催化剂，其制备方法和使用其生产氢气
公开(公告)号：WO1996006675A1
公开(公告)日：1996-03-07
申请号：PCT/KR1995000110
申请日：1995-08-29
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , PARK, Dae, Chul , CHUNG, Kyeong, Hwan , CHANG, Duck, Rye
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： B01J23/20
CPC分类号： C01B3/065 , B01J23/20 , C01B13/0207 , Y02E60/362
摘要： There is disclosed a photocatalyst for the preparation of hydrogen consisting of a catalytically active ingredient cesium (Cs) impregnated in a support K4Nb6O17, represented by the formula (I): Cs(a)/K4Nb6O17, wherein a in parenthesis denotes the amout of the catalytically active ingredient Cs impregnated in the support K4Nb6O17 and has a value of 0.05 to 5.0 % by weight based on the total weight of the support. It is prepared by combining K2CO3 with Nb2O5 in a mole ratio of 2:3 of K2CO3:Nb2O5 sintering the combination at a temperature of about 1,200 to 1,300 DEG C, to give K4Nb6O17, a support; and impregnating the support with a catalytically active inorganic ingredient Cs. Hydrogen is efficiently produced by illuminating an ultraviolet on an aqueous solution added with an oxygen-containing organic promoter at a reaction temperature of about 15 to 80 DEG C under a reaction pressure of about 0.1 to 3 atm, in the presence of the photocatalyst.
摘要翻译：公开了一种用于制备氢的光催化剂，其由浸渍在由式（I）表示的载体K4Nb6O17中的催化活性成分铯（Cs）组成：Cs（a）/ K4Nb6O17，其中括号中的a表示催化活性成分Cs浸渍在载体K4Nb6O17中，并且其值为载体总重量的0.05-5.0重量％。通过将K 2 CO 3与Nb 2 O 5以摩尔比为2:3的K 2 CO 3 :Nb 2 O 5的摩尔比组合制备，在约1,200至1300℃的温度下烧结组合，得到K4Nb6O17，载体; 并用催化活性无机成分Cs浸渍载体。在光催化剂存在下，在约15〜80℃的反应温度下，在约0.1〜3atm的反应压力下，在添加有含氧有机助催化剂的水溶液上照射紫外线来有效地制造氢。

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