ω-Iodopentyl formate | 91712-74-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: ω-Iodopentyl formate
• 英文别名: 5-iodopentyl formate
• CAS: 91712-74-2
• 化学式: C₆H₁₁IO₂
• 分子量: 242.057
• InChiKey: TYGQYERQCOBMNB-UHFFFAOYSA-N

物化性质

• 沸点：
  223.9±23.0 °C(Predicted)
• 密度：
  1.612±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  9
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  环氧己烷 在 碘 、 mercury(II) oxide 作用下， 以 苯 为溶剂， 反应 8.0h， 以15%的产率得到ω-Iodopentyl formate
  参考文献：
  名称：

  Suginome, Hiroshi; Wang, Jian Bo, Journal of the Chemical Society. Perkin transactions I, 1990, # 10, p. 2825 - 2829

  摘要：

  DOI：

文献信息

• 3-(4,5-Dihydroisoxaxol-5-yl)benzoylcyclohexenones and the use thereof as herbicides
  申请人：——

  公开号：US20030199699A1

  公开（公告）日：2003-10-23

  The invention relates to 3-(4,5-dihydroisoxazole-5-yl)benzoylcyclohexenones of the general formula (I), wherein the variables have the following meanings: R 1 , R 2 represents hydrogen, nitro, halogen, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkysulfonyl or C 1 -C 6 haloalkylsulfonyl; R 3 represents hydrogen, halogen or alkyl; R 4 represents hydrogen or alkyl; R 5 , R 6 represents hydrogen, halogen, cyano, nitro, alkyl, alkoxy, alkylthio, dialkylamino, phenyl, benzyl or carbonyl, wherein the 7 last residues can be substituted; R 11 represents optionally substituted cyclohexenone that is linked in the 2 position and that carries a hydroxy residue or derivatives thereof in the 1 position. The invention further relates to the agriculturally useful salts thereof, to methods for producing the 3-(4,5-dihydroisoxazole-5-yl)benzoylcyclohexenones, to agents that contain the inventive compound, and to the use of said derivatives or agents containing them for controlling undesired plants.

  该发明涉及通式（I）的3-(4,5-二氢异噁唑-5-基)苯甲酰环己烯酮，其中变量具有以下含义：R1，R2代表氢、硝基、卤素、氰基、烷基、卤代烷基、烷氧基、卤代烷氧基、烷硫基、卤代烷硫基、烷基磺酰基、卤代烷基磺酰基或C1-C6卤代烷基磺酰基；R3代表氢、卤素或烷基；R4代表氢或烷基；R5，R6代表氢、卤素、氰基、硝基、烷基、烷氧基、烷硫基、二烷基氨基、苯基、苄基或羰基，其中最后7个残基可以被取代；R11代表在2位连接的可选择取代的环己烯酮，在1位携带一个羟基残基或其衍生物。该发明还涉及其农业上有用的盐，生产3-(4,5-二氢异噁唑-5-基)苯甲酰环己烯酮的方法，含有该创新化合物的药剂，以及用于控制不受欢迎植物的衍生物或含有它们的药剂的用途。
• TRICYCLIC BENZOYLPYRAZOLE DERIVATIVES
  申请人：Witschel Matthias

  公开号：US20070197393A1

  公开（公告）日：2007-08-23

  Tricyclic benzoylpyrazole derivatives of the formula I where: X is oxygen, sulfur, S═O, S(═O) 2 , CR 6 R 7 , NR 8 or a bond; Y together with the two carbons to which it is attached forms a saturated, partially saturated or unsaturated 5- or 6-membered heterocycle; R 1 , R 2 , R 6 , R 7 are hydrogen, alkyl, haloalkyl, alkoxy or haloalkoxy; R 3 is halogen, alkyl, haloalkyl, alkoxy or haloalkoxy; R 4 is hydrogen, nitro, halogen, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, unsubstituted or substituted aminosulfonyl or unsubstituted or substituted sulfonylamino; R 5 is hydrogen, alkyl or halogen; l is 0, 1 or 2; R 8 is hydrogen, alkyl, haloalkyl, alkylcarbonyl, formyl, alkoxycarbonyl, haloalkoxycarbonyl, alkylsulfonyl or haloalkylsulfonyl; R 9 is substituted pyrazol-4-ylcarbonyl or substituted 5-oxopyrazolin-4-ylmethylidene; and their agriculturally useful salts; processes and intermediates for preparing the tricyclic benzoylpyrazole derivatives; compositions comprising them and the use of these derivatives or of the compositions comprising them for controlling undesirable plants are described.

  化合物I的三环苯甲酰吡唑衍生物的公式为：其中：X是氧、硫、S═O、S（═O）2、CR6R7、NR8或键；Y与其连接的两个碳原子形成饱和、部分饱和或不饱和的5-或6元杂环；R1、R2、R6、R7为氢、烷基、卤代烷基、烷氧基或卤代烷氧基；R3为卤素、烷基、卤代烷基、烷氧基或卤代烷氧基；R4为氢、硝基、卤素、氰基、烷基、卤代烷基、烷氧基、卤代烷氧基、烷基硫基、卤代烷基硫基、烷基亚磺酰基、卤代烷基亚磺酰基、烷基磺酰基、卤代烷基磺酰基、未取代或取代的氨基磺酰基或未取代或取代的磺酰胺基；R5为氢、烷基或卤素；l为0、1或2；R8为氢、烷基、卤代烷基、烷基羰基、甲酰基、烷氧羰基、卤代烷氧羰基、烷基磺酰基或卤代烷基磺酰基；R9为取代的吡唑-4-基羰基或取代的5-氧代吡唑-4-基甲基亚胺基；以及它们的农业有用盐；描述了制备这些三环苯甲酰吡唑衍生物的过程和中间体；包含它们的组合物以及使用这些衍生物或包含它们的组合物来控制不良植物的用途。
• [DE] SUBSTITUIERTE 2-BENZ(O)YLPYRIDIN DERIVATE, DEREN HERSTELLUNG UND DEREN VERWENDUNG ALS HERBIZIDE<br/>[EN] SUBSTITUTED 2-BENZ(O)YLPYRIDINES, THEIR PREPARATION AND THEIR USE AS HERBICIDES<br/>[FR] DERIVES DE 2-BENZ(O)YLPYRIDINES SUBSTITUEES, LEUR PREPARATION ET LEUR UTILISATION COMME HERBICIDES
  申请人：BASF AKTIENGESELLSCHAFT

  公开号：WO1998042671A1

  公开（公告）日：1998-10-01

  (DE) Substituierte 2-Benz(o)ylpyridine der Formel (I) und deren Salze, wobei n = 0, 1; x = CO, CH2, CH(C1-C4-Alkyl), CH-OH, CH-CN, CH-Halogen, C(Halogen)2, CH-CONH2, CH-CO-O(C1-C4-Alkyl), CH-O(C1-C4-Alkyl), C(CN) (C1-C4-Alkyl); R1 = Halogen, C1-C4-Halogenalkyl, C1-C4-Alkylthio, C1-C4-Alkylsulfinyl, C1-C4-Alkylsulfonyl; R2 = H, Halogen; R3 = H, NO2, OH, Halogen, C1-C4-Alkoxy; R4 = H, NO2, OH, Halogen, C1-C4-Alkyl, C1-C4-Halogenalkyl, C1-C4-Alkoxy; R5 = H, NO2, CN, Halogen, C1-C8-Alkyl, C3-C8-Alkenyl, C3-C8-Alkinyl, C3-C8-Cycloalkyl, C1-C8-Halogenalkyl, C2-C8-Halogenalkenyl, C2-C8-Halogenalkinyl, C1-C4-Alkoxy-C1-C4-alkyl, C2-C4-Alkenyloxy-C1-C4-alkyl, C2-C4-Alkinyloxy-C1-C4-alkyl, C1-C4-Alkylthio-C1-C4-alkyl, C1-C4-Alkylsulfinyl-C1-C4-alkyl, C1-C4-Alkylsulfonyl-C1-C4-alkyl, Cyano-C1-C8-alkyl, Cyano-C2-C8-alkenyl, Cyano-C3-C8-alkinyl, gegebenenfalls substituiertes OH, SH, SO-H, -SO2-H, COOH oder NH-COOH, -SO2Cl, -N(R9, R10), -NH-SO2-(C1-C8-Alkyl), -N[-SO2-(C1-C8-Alkyl)]2, -N(C1-C8-Alkyl) [-SO2-(C1-C8-Alkyl)], -SO2-N(R9, R10), -O-CO-NH-R9, geg. subst. CHO, -O-CHO oder -NH-CHO, -NH-CO-NH-R9, -O-CS-NH2, -OCS-N(C1-C8-Alkyl)2, -CO-N(R9, R10), -CS-N(R9, R10), -CO-NH-SO2-(C1-C4-Alkyl), -CO-N(C1-C4-Alkyl)-SO2-(C1-C4-Alkyl), Hydroxycarbonyl-C1-C8-alkyl, (C1-C8-Alkoxy)carbonyl-C1-C6-alkyl, -CH2-CH(Halogen)-CO-N(R9, R10), -CH2-CH(Halogen)-CN, -CH2-CH(Halogen)-CO-(C1-C4-Alkyl), geg. subst. -CH2-CH(Halogen-COOH, -CH=C(Halogen)-COOH oder -CH=C(C1-C4-Alkyl)-COOH, geg. subst. -CH=N-OH oder -CH(-Y-R15, -Z-R15), (II) oder (III); R9, R10 = H, C1-C8-Alkyl, C3-C8-Cycloalkyl, C2-C8-Alkenyl, C3-C8-Alkinyl, C1-C8-Halogenalkyl, C1-C4-Alkoxy-C1-C4-alkyl, C1-C4-Alkylthio-C1-C4-alkyl, C1-C4-Alkylsulfinyl-C1-C4-alkyl, C1-C4-Alkylsulfonyl-C1-C4-alkyl, Cyano-C1-C8-alkyl, Hydroxycarbonyl-C1-C4-alkyl, (C1-C4-Alkoxy)carbonyl-C1-C4-alkyl, (C3-C6-Cycloalkoxy)carbonyl-C1-C4-alkyl, (C1-C4-Alkoxy)carbonyl-C3-C7-cycloalkyl, C1-C4-Alkoxy-(C1-C4-alkoxy)carbonyl-C1-C4-alkyl, C1-C6-Alkoxy, gegebenenfalls substituiertes Phenyl oder Phenyl-C1-C4-alkyl, oder R9 + R10 zusammen = gegebenenfalls substituierte Tetramethylen-, Pentamethylen- oder Ethylenoxyethylenkette; Y, Z = O, S; R15 = C1-C8-Alkyl, C1-C8-Halogenalkyl, C1-C4-Alkoxy-C1-C4-alkyl; R16-R21 = H, CN, C1-C8-Alkyl, C1-C4-Alkoxy-C1-C4-alkyl, C1-C8-Alkoxy, C1-C4-Alkoxy-C1-C4-alkoxy, COOH, (C1-C8-Alkoxy)carbonyl, CONH2, (C1-C8-Alkyl)aminocarbonyl, Di(C1-C8-Alkyl)aminocarbonyl; R6 = H, NO2, Halogen, gegebenenfalls substituiertes OH oder COOH; R7 = H, NO2, Halogen, gegebenenfalls substituiertes OH; ausgenommen diejenigen Verbindungen (I), bei denen X = CH2 und R5 = geg. subst. OH sowie R3, R7 = H oder R1 = Halogen sowie R3, R4, R6, R7 = H; Verwendung: als Herbizide; zur Desikkation/Defoliation von Pflanzen.(EN) Substituted 2-benz(o)ylpyridines of formula (I) and the salts thereof, wherein n = 0, 1; x = CO, CH2, CH(C1-C4-alkyl), CH-OH, CH-CN, CH-halogen, C(halogen)2, CH-CONH2, CH-CO-O(C1-C4-alkyl), CH-O(C1-C4-alkyl), C(CN) (C1-C4-alkyl); R1 = halogen, C1-C4-halogen alkane, C1-C4-alkylthio, C1-C4-alkyl sulfinyl, C1-C4-alkyl sulfonyl; R2 = H, halogen; R3 = H, NO2, OH, halogen, C1-C4-alkoxy; R4 = H, NO2, OH, halogen, C1-C4-alkyl, C1-C4 halogen alkane, C1-C4-alkoxy; R5 = H, NO2, CN, halogen, C1-C8-alkyl, C3-C8-alkenyl,C3-C8-alkinyl, C3-C8-cycloalkyl, C1-C8-halogen alkane, C2-C8-halogen alkenyl, C2-C8-halogen alkane, C1-C4-alkoxy-C1-C4-alkyl, C2-C4-alkenyloxy-C1-C4-alkyl, C2-C4-alkinyloxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, cyano-C1-C8-alkyl, cyano-C2-C8-alkenyl, cyano-C3-C8-alkinyl, optionally substituted OH, SH, SO-H, -SO2-H, COOH or NH-COOH, -SO2Cl, -N(R9, R10), -NH-SO2-(C1-C8-alkyl), -N[-SO2-(C1-C8-alkyl)]2, -N(C1-C8-alkyl) [-SO2-(C1-C8-alkyl)], -SO2-N(R9, R10), -O-CO-NH-R9, optionally substituted CHO, -O-CHO or -NH-CHO, NH-CO-NH-R9, -O-CS-NH2, -OCS-N(C1-C8-alkyl)2, -CO-N(R9, R10), -CS-N (R9, R10), -CO-NH-SO2-(C1-C4-alkyl), -CO-N(C1-C4-alkyl), -SO2-(C1-C4-alkyl), hydroxycarbonyl-C1-C8-alkyl, (C1-C8-alkoxy)carbonyl-C1-C6-alkyl, -CH2-CH(halogen)-CO-N(R9, R10), -CH2-CH(halogen)-CN, -CH2-CH(halogen)-CO-(C1-C4-alkyl), optionally substituted -CH2-CH(halogen-COOH, -CH=C(halogen)-COOH or -CH=C(C1-C4-alkyl)-COOH, optionally substituted -CH=N-OH or -CH(-Y-R15, -Z-R15), (II) or (III); R9, R10 = H, C1-C8-alkyl, C3-C8-cycloalkyl, C2-C8-alkenyl, C3-C8-alkinyl, C1-C8-halogen alkane, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, cyano-C1-C8-alkyl, hydroxycarbonyl-C1-C4-alkyl, (C1-C4-alkoxy)carbonyl-C1-C4-alkyl, (C3-C6-cycloalkoxy)carbonyl-C1-C4-alkyl, (C1-C4-alkoxy)carbonyl-C3-C7-cycloalkyl, C1-C4-alkoxy-(C1-C4)alkoxy)-carbonyl-C1-C4-alkyl, C1-C6-alkoxy, optionally substituted phenyl or phenyl-C1-C4-alkyl or R9 + R10 together = optionally substituted tetramethylene, pentamethylene or ethylene oxyethylene chain; Y, Z = O, S; R15 = C1-C8-alkyl, C1-C8 halogen alkane, C1-C4-alkoxy-C1-C4-alkyl; R16-R21 = H, CN, C1-C8-alkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C8-alkoxy, C1-C4-alkoxy-C1-C4-alkoxy, COOH, (C1-C8-alkoxy)carbonyl, CONH2, (C1-C8-alkyl)aminocarbonyl, di(C1-C8-alkyl)aminocarbonyl; R6 = H, NO2, halogen, optionally substituted OH or COOH; R7 = H, NO2, halogen, optionally substituted OH; excluding those compounds in (I) in wherein X = CH2 and R5 = optionally substituted OH as well as R3, R7 = H or R1 = halogen as well as R3, R4, R6, R7 = H. The invention further relates to the use of said substances as herbicides and for dessication/defoliation of plants.(FR) L'invention concerne des 2-benz(o)ylpyridines substituées de la formule (I) et leurs sels, formule dans laquelle n = 0, 1; X = CO, CH2, CH(alkyle C1-C4), CH-OH, CH-CN, CH-halogène, C(halogène)2, CH-CONH2, CH-CO-O-(alkyle C1-C4), CH-O-(alkyle C1-C4), C(CN)(alkyle C1-C4); R1 = halogène, halogénure d'alkyle C1-C4, alkylthio C1-C4, alkylsulfinyle C1-C4, alkylesulfonyle C1-C4; R2 = H, halogène; R3 = H, NO2, HO, halogène, alcoxy C1-C4; R4 = H, NO2, OH, halogène, alkyle C1-C4, halogénure d'alykle C1-C4, alcoxy C1-C4; R5 = H, NO2, CN, Halogène, alkyle C1-C8, alkényle C3-C8, alkinyle C3-C8, cycloalkyle C3-C8, halogénure d'alkyle C1-C8, halogénure d'alkényle C2-C8, halogénure d'alkinyle C2-C8, alcoxy C1-C4-alkyle C1-C4, alkényloxy C2-C4-alkyle C1-C4, alkinyloxy C2-C4-alkyle C1-C4, alkylthio C1-C4-alkyle C1-C4, alkylsulfinyle C1-C4-alkyle C1-C4, alkylesulfonyle C1-C4-alkyle C1-C4, cyano-alkyle C1-C8, cyano-alkényle C2-C8, cyano-alkinyle C3C8, OH éventuellement subst., SH, SO-H, SO2H, COOH ou NH-COOH, -SO2Cl, -N(R9, R10), -NH-SO2-(alkyle C1-C8), -N[-SO2-alkyle C1-C8)]2, N-(alkyle C1-C8) [-SO2-(alkyle C1-C8)], -SO2-N(R9, R10), -O-CO-NH-R9, CHO éventuel. subst., -O-CHO ou -NH-CHO, -NH-CO-NH-R9, -O-CS-NH2, -O-CS-N(alkyle C1-C8)2, -CO-N(R9, R10), -CS-N(R9, R10), -CO-NH-SO2(alkyle C1-C4), -CO-N(alkyle C1-C4)-SO2(alkyle C1-C4), hydroxycarbonyle-alkyle C1-C8, (alcoxy C1-C8)carbonyle-alkyle C1-C6, -CH2-CH(halogène)-CO-N(R9, R10), -CH2-CH(halogène)-CN, -CH2-CH(halogène)-CO-(alkyle C1-C4), -CH2-CH(halogène) éventuel. subst., -CH=C(halogène)-COOH ou -CH=C(alkyle C1-C4)-COOH, -CH=N-OH éventuel. susbt. ou -CH(-Y-R15, -Z-R15), (II) ou (III); R9, R10 = H, alkyle C1-C8, cycloalkyle C3-C8, alkényle C2-C8, alkinyle C3-C8, halogénure d'alkyle C3-C8, alcoxy C1-C4-alkyle C1-C4, alkylthio C1-C4-alkyle C1-C4, alkylesulfinyle C1-C4-alkyle C1-C4, alkylesulfonyle C1-C4-akyle C1-C4, cyano-alkyle C1-C8, hydroxycarbonyle-alkyle C1-C4, (alcoxy C1-C4)carbonyle-alkyle C1-C4, (cycloalcoxy C3-C6)carbonyle-alkyle C1-C4, (alcoxy C1-C4)carbonyle-cycloalkyle C3-C7), alcoxy C1-C4-(alcoxy C1-C4)carbonyle-alkyle C1-C4, alcoxy C1-C6, phényle éventuellement substitué ou phényle-alkyle C1-C4, ou R9 + R10 conjointement = chaîne tétraméthylène, pentaméthylène ou éthalène-oxyéthylène éventuellement substituée; Y, Z = O, S; R15 = alkyle C1-C8, halogénure d'alkyle C1-C8, alcoxy C1-C4-alkyle C1-C4; R16 - R21 = H, CN, alkyle C1-C8, alcoxy C1-C4-alkyle C1-C4, alcoxy C1-C8, alcoxy C1-C4-alcoxy C1-C4, COOH, (alcoxy C1-C8)carbonyle, CONH2, (alkyle C1-C8)aminocarbonyle, di(alkyle C1-C8)aminocarbonyle; R6 = H, NO2, halogène, OH éventuellement substitué ou COOH; R7 = H, NO2, halogène, OH éventuellement substitué; à l'exception des composés (I) où X = CH2 et - R5 = OH éventuel. subst., ainsi que R3, R7 = H ou - R1 = halogène, ainsi que R3, R4, R6, R7 = H. Ces composés s'utilisent comme herbicides, ainsi que pour la dessiccation/défoliation de plantes.

  Les substitués 2-benzo pyridines de la formula (I) et leurs acides salts, où n = 0, 1; x = CO, CH2, CH(C1-C4-alkyl), CH-OH, CH-CN, CH-halogen, C(halogen)2, CH-CONH2, CH-CO-O(C1-C4-alkyl), CH-O(C1-C4-alkyl), C(CN) (C1-C4-alkyl), R1 = halogen, C1-C4-halogen alkane, C1-C4-alkylthio, C1-C4-alkylsulfinyl, C1-C4-alkylesulfonyle, R2 = H, halogen, R3 = H, NO2, OH, halogen, C1-C4-alkoxy, R4 = H, NO2, OH, halogen, C1-C4-alkyl, C1-C4 halogen alkane, C1-C4-alkoxy, R5 = H, NO2, CN, halogen, C1-C4-alkyl, C3-C8-alkenyl, C3-C8-alkinyl, C3-C8-cycloalkyl, C1-C8-halogen alkyl, C2-C8-halogen alkene, C2-C8-halogen alkyl, C1-C4-alkoxy-C1-C4-alkyl, C2-C4-alkenyloxy-C1-C4-alkyl, C2-C4-alkinyloxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkylesulfonyle-C1-C4-alkyl, cyano-C1-C8-alkyl, cyano-C2-C8-alkenyl, cyano-C3-C8-alkinyl, OH ousubst. SH, SO-H, -SO2-H, COOH ou NH-COOH, -SO2Cl, -N(R9, R10), -NH-SO2-(C1-C8-alkyl), -N[-SO2-(C1-C8-alkyl)]2, -N (C1-C8-alkyl) [-SO2-(C1-C8-alkyl)], -SO2-N(R9, R10), -O-CO-NH-R9, élément experiments. CHO ousubst. -O-CHO ou -NH-CHO, NH-CO-NH-R9, -O-CS-NH2, -O-CS-N( C1-C8-alkyl )2, -CO-N(R9, R10), -CS-N(R9, R10), -CO-NH-SO2-(C1-C4-alkyl), -CO-N (C1-C4-alkyl) SO2 - (C1-C4-alkyl ), Hydroxycarbonyl-C1-C8-alkyl, (C1-C8-alkoxy)carbonyl-C1-C6-alkyl, -CH2-CH(halogen)-CO-N(R9, R10), -CH2-CH(halogen)-CN, -CH2-CH(halogen)-CO-(C1-C4-alkyl), -CH2-CH(halogen)-COON, -CH2-CH-halogen-COOH ou ), -CH=N-OH ousubst. -CH(-Y-R15, -Z-R15), (II) ou (III); R9, R10 = H, C1-C8-alkyl, C3-C8-cycloalkyl, C2-C8-alkenyl, C3-C8-alkinyl, C1-C8-halogen alkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkyle sulfonyle-C1-C4-alkyl, C1-C4-alkynesulfenyl-C1-C4-alkyl, cyano-C1-C8-alkyl, hydroxycarbonyl-C1-C4-alkyl, (C1-C4-alkoxy)carbonyl-C1-C4-alkyl, (C3-C6-cycloalkoxy)carbonyl-C1-C4-alkyl, (C1-C4-alkoxy)carbonyl-C3-C7-cycloalkyl, C1-C4-alkoxy-(C1-C4-exalkoxy)-carbonyl-C1-C4-alkyl, C1-C6-alkoxy, optionnellement substitué phényle ou phényle-alkyl C1-C4, ou R9 + R10 ensemble = optionnellement substitué tétraméthylène, pentaméthylène ou éthylène-oxyéthylène; Y, Z = O, S; R15 = C1-C8-alkyl, C1-C8-halogen alkyl, C1-C4-alkoxy-C1-C4-alkyl; R16 à R21 = H, CN, C1-C8-alkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C8-alkoxy, C1-C4-alkoxy-C1-C4-alkoxy, COOH, (C1-C8-alkoxy)carbonyl, CONH₂, (C1-C8-alkyl)aminocarbonyl, di( C1-C8-alkyl )aminocarbonyl; R6 = H, NO₂, halogen, OH ou substitution. COOH; R7 = H, NO₂, halogen, OH ou substitution; à l'exception des composés (I) où X = CH₂ et R5 = OH ou substitution. ainsi que R3, R7 = H ou R1 = halogen, ainsi que R3, R4, R6, R7 = H. Ces composés sont utilisés comme acides herbicides et pour la dessication/ défoliation des plantes.
• Photoinduced transformations. Part 73. Transformations of five- (and six-) membered cyclic alcohols into five- (and six-) membered cyclic ethers - a new method of a two-step transformation of hydroxy steroids into oxasteroids
  作者：Hiroshi Suginome、Shinji Yamada

  DOI：10.1021/jo00194a015

  日期：1984.10
• SUBSTITUIERTE 2-BENZ(O)YLPYRIDIN DERIVATE, DEREN HERSTELLUNG UND DEREN VERWENDUNG ALS HERBIZIDE
  申请人：BASF AKTIENGESELLSCHAFT

  公开号：EP0968188A1

  公开（公告）日：2000-01-05