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序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
81 JPS5511647B2 - JP3108174 1974-03-20 JPS5511647B2 1980-03-26
82 JPS544928B2 - JP194475 1974-12-25 JPS544928B2 1979-03-12
83 JPS541300B1 - JP9125670 1970-10-17 JPS541300B1 1979-01-23
84 Method of accelerating base-catalyzed, ionic, organic reactions JP8211876 1976-07-09 JPS537603A 1978-01-24 YOSHIMURA NORIAKI; TAMURA MASUHIKO
PURPOSE: To effectively and economically accelerate org. ionic reactions which proceed in on org. liquid in the presence of a basic alkali metal compound as catalyst, by the addition of a certain polyoxyalkylene derivative. COPYRIGHT: (C)1978,JPO&Japio
85 Method of producing alpha*betaaunsaturated alcohol selectively JP15480475 1975-12-26 JPS5278810A 1977-07-02 OZAKI ATSUMU; MIZOROGI TSUTOMU; MEGURO SHIYUNICHI
86 Fuhowaarudehidoto fuhowaarukoorutono joryubunriho JP2406075 1975-02-28 JPS51100008A 1976-09-03 ICHIKAWA YATARO; YAMANAKA YOSHUKI; SUZUKI MASAO; SAWAKI TOORU
87 Chikanaruriruesuteruno seiho JP1590775 1975-02-08 JPS5168515A 1976-06-14 UERUNAA AKUIRA; WARUTAA HIMUMERE; KURUTO SHUNAIDAA
88 Fuhowaarukooru no seizoho JP11164374 1974-09-30 JPS5139616A 1976-04-02 ICHIKAWA YATARO; KOBAYASHI OSAMU; SOMA KAZUHIKO; YAMANAKA YOSHUKI; SUZUKI MASAO; SEICHI TATSUYUKI
89 JPS50157307A - JP6283774 1974-06-05 JPS50157307A 1975-12-19
90 JPS5010565B1 - JP3201770 1970-04-16 JPS5010565B1 1975-04-22
91 UTILISATION DE CERTAINES PLANTES HYPERACCUMULATRICES DE MÉTAUX DE TRANSITION POUR DES RÉDUCTIONS DE COMPOSÉS ORGANIQUES PAR VOIES VERTES EP15763379.3 2015-07-15 EP3177399A1 2017-06-14 GRISON, Claude; ESCANDE, Vincent
The invention relates to a method for reducing organic compounds using catalysts containing nickel (O) from metal hyperaccumulator plants. Said method can be implemented in a green manner and is advantageous compared to methods using the known catalysts.
92 Funktionalisierte RGD-Peptidmimetika und deren Herstellung sowie Implantat mit einer Beschichtung, die solche funktionalisierte RGD-Peptidmimetika enthält EP11188034.0 2011-11-07 EP2452703B1 2015-03-04 Borck, Alexander; Gratz, Matthias; Kessler, Horst; Joner, Michael; Rechenmacher, Florian; Neubauer, Stefanie
93 Funktionalisierte RGD-Peptidmimetika und deren Herstellung sowie Implantat mit einer Beschichtung, die solche funktionalisierte RGD-Peptidmimetika enthält EP11185761.1 2011-10-19 EP2452702B1 2015-03-04 Borck, Alexander; Gratz, Matthias; Kessler, Horst; Joner, Michael; Rechenmacher, Florian; Neubauer, Stefanie
94 METHOD FOR PRODUCING BUTANOL USING EXTRACTIVE FERMENTATION WITH OSMOLYTE ADDITION EP10784647.9 2010-11-23 EP2504447A2 2012-10-03 PATNAIK, Ranjan; GRADY, Michael, Charles
A method is provided for producing butanol through microbial fermentation, in which the butanol product is removed during the fermentation by extraction into a water-immiscible organic extractant in the presence of at least one osmolyte at a concentration at least sufficient to increase the butanol partition coefficient relative to that in the presence of the osmolyte concentration of the basal fermentation medium and of an optional fermentable carbon source. The osmolyte may comprise a monosaccharide, a disaccharide, glycerol, sugarcane juice, molasses, polyethylene glycol, dextran, high fructose corn syrup, corn mash, starch, cellulose, and combinations thereof. Also provided is a method and composition for recovering butanol from a fermentation medium.
95 METHOD FOR PRODUCING BUTANOL USING EXTRACTIVE FERMENTATION WITH ELECTROLYTE ADDITION EP10782795.8 2010-11-23 EP2504446A1 2012-10-03 GRADY, Michael, Charles; PATNAIK, Ranjan
A method for producing butanol through microbial fermentation, in which the butanol product is removed during the fermentation by extraction into a water-immiscible organic extractant in the presence of at least one electrolyte at a concentration at least sufficient to increase the butanol partition coefficient relative to that in the presence of the salt concentration of the basal fermentation medium, is provided. The electrolyte may comprise a salt which dissociates in the fermentation medium, or in the aqueous phase of a biphasic fermentation medium, to form free ions. Also provided is a method and composition for recovering butanol from a fermentation medium.
96 Pyranderivative mit exocyclischer Doppelbindung EP04010545.4 2004-05-04 EP1482020B1 2006-09-06 Poetsch, Eike; Meyer, Volker; Binder, Werner; Heckmeier, Michael; Lüssem, Georg; Gürtler, Stephan
97 Substituted glutaric acid lactones in the treatment of hyperlipidemia EP86103068.2 1986-03-07 EP0194610A1 1986-09-17 Baran, John Stanislaus; Lindberg, Thomas James; Lowrie, Harman Smith

The invention relates to compounds of formula I wherein R represents lower alkyl, cycloalkyl aryl, or a group of the formula of the formula cycloalkyl or phenyl; wherein R cycloalkyl or phenyl; m is an integer from 8 to 15, inclusive; and the pharmaceutically acceptable salts or esters thereof, which are useful to inhibit the formation of serum cholesterol by virtue of their ability to inhibit β-hydroxy-β-methylglutaryl-CoA(HMG CoA), the rate-controlling substance in the synthesis of serum cholesterol.

98 Azolyl derivatives as fungicides EP83300033 1983-01-05 EP0089100A3 1984-07-11 Marchington, Anthony Frank; Lewis, Timothy; Clough, John Martin; Worthington, Paul Anthony; Griffin, David Alan; Dalziel, John

Compounds of formula: and stereoisomers thereof, wherein W is -CH= or =N-; Q is optionally substituted aryl, especially optionally substituted phenyl, optionally substituted aralkyl or alkyl; R', R2, R3, R4, R5 and R6, which may be the same or different, are H, optionally substituted alkyl, cycloalkyl, aralkyl or optionally substituted phenyl; and R7 and R3 and H, alkyl or optionally substituted phenyl; and acid salts and metal complexes thereof; have fungicidal and plant growth regulating activity.

99 MICROORGANISMS AND METHODS FOR PRODUCTION OF SPECIFIC LENGTH FATTY ALCOHOLS AND RELATED COMPOUNDS EP13846388 2013-10-14 EP2906705A4 2016-09-07 OSTERHOUT ROBIN E; BURGARD ANTHONY P
100 MICROORGANISMS AND METHODS FOR PRODUCTION OF SPECIFIC LENGTH FATTY ALCOHOLS AND RELATED COMPOUNDS EP13846388.0 2013-10-14 EP2906705A1 2015-08-19 OSTERHOUT, Robin, E.; BURGARD, Anthony, P.
The invention provides non-naturally occurring microbial organisms containing a fatty alcohol, fatty aldehyde or fatty acid pathway, wherein the microbial organisms selectively produce a fatty alcohol, fatty aldehyde or fatty acid of a specified length. Also provided are non-naturally occurring microbial organisms having a fatty alcohol, fatty aldehyde or fatty acid pathway, wherein the microbial organisms further include an acetyl-CoA pathway. In some aspects, the microbial organisms of the invention have select gene disruptions or enzyme attenuations that increase production of fatty alcohols, fatty aldehydes or fatty acids. The invention additionally provides methods of using the above microbial organisms to produce a fatty alcohol, a fatty aldehyde or a fatty acid.
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