序号 | 专利名 | 申请号 | 申请日 | 公开(公告)号 | 公开(公告)日 | 发明人 |
---|---|---|---|---|---|---|
241 | NOVEL NITROSATION POLYMER IN ORGANIC SYNTHESIS | AU2003264272 | 2003-09-06 | AU2003264272A1 | 2004-04-23 | ROCHE DIDIER; LARDY CLAUDE |
242 | New polymer nitrosation organic synthesis | FR0212136 | 2002-10-01 | FR2845090A1 | 2004-04-02 | ROCHE DIDIER; LARDY CLAUDE |
La présente invention a pour objet un nouveau polymère de nitrosation de formuledans laquelle X, Y, R1, R2 et R3 sont tels que définis dans la revendication 1. Elle concerne également un procédé de préparation dudit polymère. | ||||||
243 | Plant ethylene response inhibition compounds and complexes | AU4850999 | 1999-06-30 | AU768290B2 | 2003-12-04 | DALY JAMES; KOURELIS BOB |
244 | COMPUESTOS Y COMPLEJOS PARA LA INHIBICION DE RESPUESTA AL ETILENO EN PLANTAS. | MXPA01001825 | 1999-06-30 | MXPA01001825A | 2003-06-18 | DALY JAMES |
La presente invencion generalmente esta relacionada con la regulacion de la fisiologia de la planta, en particular con metodos para inhibir la respuesta de etileno en plantas o productos de las plantas, y tiene tres modalidades. La primera modalidad se relaciona con metodos para minimizar impurezas capaces de ajustarse reversiblemente a sitios receptores de etileno en plantas durante la sintesis de ciclopropeno y sus derivados tales como metilciclopropeno, evitando de esta forma los efectos negativos que estas impurezas tienen en las plantas tratadas con ciclopropeno y sus derivados. La segunda modalidad se relaciona con complejos formados de agentes de encapsulacion molecular tales como ciclodextrina y cilopropeno y sus derivados, tales como metilciclopropeno, en adicion a ciclopentadieno y diazociclopentadieno y sus derivados, proporcionando de esta forma medios convenientes para almacenar y transportar estos compuestos capaces de inhibir la respuesta al etileno en plantas, las cuales son gases reactivos y altamente inestables debido a la oxidacion y otras reacciones potenciales. La tercera modalidad se relaciona con metodos convenientes de aplicacion en plantas de estos compuestos los cuales son capaces de inhibir la respuesta al etileno en las plantas para extender su vida en anaquel. | ||||||
245 | NOVEL DIAZO DERIVATIVES AND PROCESS FOR THEIR PREPARATION | CA2392282 | 2002-07-03 | CA2392282A1 | 2003-01-04 | VERARDO GIANCARLO; GIUMANINI ANGELO; GORASSINI ANDREA; ZAPPALA ANTONIO |
Novel diazo derivatives useful for the deacidification of paper material and the process for their preparation comprising three steps starting from an amine and ethyl chlorocarbonate, are described. | ||||||
246 | PLANT ETHYLENE RESPONSE INHIBITION COMPOUNDS AND COMPLEXES | BG10530801 | 2001-03-05 | BG105308A | 2002-04-30 | DALY JAMES; KOURELIS BOB |
The present invention generally relates to the regulation of plant physiology, in particular to methods for inhibiting the ethylene response in plants or plant products, and has three embodiments. The first embodiment relates of methods of minimizing impurities capable of reversibly binding to plant ethylene receptor sites during the synthesis of cyclopropene and its derivatives such as methylcyclopropene, thereby avoiding the negative effects these impurities have on plants treated with cyclopropene and its derivatives. The second embodiment relates to complexes formed from molecular encapsulation against such as cyclodextrin, and cyclopropene and its derivatives such as methylcyclopropene, in addition to cyclopentadiene and diazocyclopentadiene and their derivatives, thereby providing a convenient means for storing and transporting these compounds, capable of inhibiting the ethylene response in plant, which are reactive gases and highly unstable because of oxidation and other potential reactions. The third embodiment relates to convenient methods of delivering to plants these compounds capable of inhibiting the ethylene responses in the plants in order to extend their shelf life. 58 claims | ||||||
247 | Azametino dyes with heterocyclic side groups. | ES96104862 | 1996-03-27 | ES2165934T3 | 2002-04-01 | SCHMIDT ANDREAS JOHANN DR; SENS RUDIGER DR |
COLORANTES DE METINA DE FORMULA EN DONDE K ES UN RADICAL CARBOCICLICO O HETEROCICLICO, X ES NITROGENO O UN RADICAL DE FORMULA CQ{SUP,1}, YQ{SUP,1}, Q{SUP,2} YQ{SUP,3} SON HIDROGENO, ALQUILO DE C{SUB,1}C{SUB,6}, QUE PUEDE ESTAR A VECES ROTO POR 1 O 2 ATOMOS DE OXIGENO CON FUNCION ETER, BENZILO, CICLOALQUILO DE C{SUB,3}C{SUB,8}, FLUOROALQUILO DE C{SUB,1}-C{SUB,4}, FENILO OPCIONALMENTE SUSTITUIDO, ALCOXI DE C{SUB,1}-C{SUB,6}, BENZILOXI, FENOXI OPCIONALMENTE SUSTITUIDO, ALQUILTIO DE C{SUB,1}-C{SUB,6}, HALOGENO, CIANO, FORMILAMINO O UN RADICAL DE FORMULA R{SUP,3}, CO-OR{SUP,1}, -CO-NHR{SUP,1}, -CO-NH-CO-R{SUP,1}, -CO-NH-COR{SUP,4}, -CO-NH-SO{SUB,2}R{SUP,4}, -NH-COR{SUP,1}, -NH-COOR{SUP,1}, -NH-CO-NR{SUP,1}R{SUP,2}, -NH-CS-OR{SUP,1}, -NH-CSNR{SUP,1}R{SUP,2}, -NH-CO-R{SUP,4}, -NH-SO{SUB,2}-R{SUP,1}, -NHSO{SUB,2}-R{SUP,4}, O -NH-SO{SUB,2}-R{SUP,1}R{SUP,2}, EN DONDE R{SUP,1} YR{SUP,2} SON ALQUILO DE C{SUB,1}-C{SUB,13}, QUE ESTA OPCIONALMENTE SUSTIUIDO, CICLOALQUILO DE C{SUB,3}-C{SUB,8}, FENILO OPCIONALMENTE SUSTITUIDO, O -NR{SUP,1}R{SUP,2} TAMBIEN PUEDE SER AMINO, R{SUP,3} ES UN RADICAL HETEROCICLICO NO AROMATICO, YR{SUP,4} ES UN RADICAL HETEROCICLICO, OQ{SUP,1} YQ{SUP,2} JUNTO CON LOS ATOMOS DE CARBONO A LOS QUE ESTAN UNIDOS, SON UN ANILLO HETEROCICLICO O CARBOCICLICO, CON LA CONDICION DE QUE AL MENOS UNO DE LOS RADICALES Q{SUP,1}, Q{SUP,2} OQ{SUP,3} TENGA EL SIGNIFICADO DEL RADICAL R{SUP,3}, Y UN PROCEDIMIENTO PARA SU TRANSFERENCIA TERMICA. | ||||||
248 | METHOD FOR REGULATION OF PLANT PHYSIOLOGY AND PLANT ETHYLENE RESPONSE INHIBITION COMPOUNDS AND COMPLEXES | IL14148599 | 1999-06-30 | IL141485A0 | 2002-03-10 | |
249 | PLANT ETHYLENE RESPONSE INHIBITION COMPOUNDS AND COMPLEXES | HRP20010121 | 2001-02-19 | HRP20010121A2 | 2002-02-28 | DALY JAMES; KOURELIS BOB |
250 | METHODS FOR PRODUCING CYCLOPROPENE DERIVATIVES, THEIR COMPLEXES AND USE OF THE LATTER | HUP0103288 | 1999-06-30 | HUP0103288A2 | 2002-01-28 | DALY JAMES; KOURELIS BOB |
251 | Compounds and complexes for inhibition of plant reaction to ethylene | CZ2001628 | 1999-06-30 | CZ2001628A3 | 2001-12-12 | DALY JAMES; KOURELIS BOB |
252 | TR200100802 | 1999-06-30 | TR200100802T2 | 2001-11-21 | DALY JAMES; KOURELIS BOB | |
253 | Plant ethylene response inhibition compounds and complexes. | ZA200101411 | 2001-02-20 | ZA200101411B | 2001-08-21 | DALY JAMES; KOURELIS BOB |
254 | Plant ethylene response inhibition compounds and complexes. | AP2001002095 | 1999-06-30 | AP2001002095A0 | 2001-03-31 | DALLY JAMES; KOURELIS BOB |
The present invention generally relates to the regulation of plant physiology, in particular to methods for inhibiting the ethylene response in plants or plant products, and has three embodiments. The first embodiment relates to methods of minimizing impurities capable of reversibly binding to plant ethylene receptor sites during the synthesis of cyclopropene and its derivatives such as methylcyclopropene, thereby avoding the negative effects these impurities have on plants treated with cyclopropene and its derivatives. The second embodiment relates to complexes formed from molecular encapsulation agents such as cyclodextrin, and cylopropene and its derivates such as methylcyclopropene, in addition to cylopentadiene and diazocyclopentadiene and their derivatives, thereby providing a convenent means for storing and transporting these compounds capable of inhibiting the ethylene response in plants, which are reactive gases and highly unstable because of oxidation and other potential reactions. The third embodiment relates to convenient methods of delivery to plants these compounds capable of inhibiting the ethylene response in the plants in order to extend their shelf life. | ||||||
255 | METHOD OF OBTAINING SUBSTITUTED BENZENES AND BENESONSULFONIC ACID AS WELL AS THEIR DERIVATIVES AND METHOD OF OBTAINING N,N'-SUBSTITUTED UREAS | PL30011993 | 1993-08-17 | PL174329B1 | 1998-07-31 | BAUMEISTER PETER; SEIFERT GOTTFRIED; STEINER HEINZ |
256 | METHOD OF OBTAINING SUBSTITUTED N-(1,3,5-TRIAZIN-AND 1,3 PYRIMIDIN-YL-2)-N'-(ALKILBENZENSULPHONYL)-(THIO)UREAS | PL31898193 | 1993-08-17 | PL173856B1 | 1998-05-29 | BAUMEISTER PETER; SEIFERT GOTTFRIED; STEINER HEINZ |
257 | PROCESS FOR THE PREPARATION OF N, N''-SUBSTITUTED UREAS | MYPI19931421 | 1993-07-20 | MY110183A | 1998-02-28 | HEINZ STEINER; GOTTFRIED SEIFERT; PETER BAUMEISTER |
A PROCESS FOR THE PREPARATION OF SUBSTITUTED BENZENESULFONIC ACID AND ITS DERIVATIVES COMPRISING DIAZOTISATION OF AN AMINOBENZENE OR ORTHO-AMINO-BENZENESULFONIC ACID DERIVATIVE FOLLOWED BY HOMOGENEOUS PALLADIUM-CATALYSED COUPLING WITH AN OLEFINE AND HETEROGENEOUS PALLADIUM-CATALYSED HYDROGENATION OF THE OLEFINIC SUBSTITUENT, WHEREIN THE HOMOGENEOUS CATALYST IS REDUCED AND PRECIPITATED AS METAL AFTER THE COUPLING IN THE REACTION MIXTURE AND USED AS A HETEROGENEOUS PALLADIUM CATALYST FOR THE HYDROGENATION STEP. THE PROCESS IS PARTICULAR SUITABLE FOR THE PREPERATION N-BENZENESULFON-N''-TRIAZINYL-UREA HERBICIDES. | ||||||
258 | A process for the preparation of substituted phenyl and Phenylsulfonsäureverbindungen and their derivatives and methods for preparing N, N-substituted ureas | DE69305711 | 1993-08-09 | DE69305711D1 | 1996-12-05 | BAUMEISTER PETER; SEIFERT GOTTFRIED; STEINER HEINZ |
259 | Cyclobutane derivatives and their use as inhibitors of prote in farnesyltransferase | AU5722796 | 1996-05-02 | AU5722796A | 1996-11-21 | ARENDSEN DAVID L; ROSENBERG SAUL H; ROCKWAY TODD W; STEIN HERMAN H; FUNG ANTHONY K L |
260 | AT93810562 | 1993-08-09 | ATE144762T1 | 1996-11-15 | BAUMEISTER PETER; SEIFERT GOTTFRIED; STEINER HEINZ | |