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Heinzmann, S: Next Level of Regionalism. Deep I...
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Erscheinungsdatum: 11.11.2018, Medium: Taschenbuch, Einband: Kartoniert / Broschiert, Titel: The Next Level of Regionalism. Deep Integration of Regio-Regio PTAs, Autor: Heinzmann, Stefan, Verlag: GRIN Verlag, Sprache: Englisch, Rubrik: Wirtschaft International, Seiten: 104, Informationen: Paperback, Gewicht: 161 gr, Verkäufer: averdo

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The Next Level of Regionalism. Deep Integration...
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The Next Level of Regionalism. Deep Integration of Regio-Regio PTAs ab 34.99 € als pdf eBook: . Aus dem Bereich: eBooks, Wirtschaft,

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The Next Level of Regionalism. Deep Integration...
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The Next Level of Regionalism. Deep Integration of Regio-Regio PTAs ab 44.99 € als Taschenbuch: . Aus dem Bereich: Bücher, Wissenschaft, Wirtschaftswissenschaft,

Anbieter: hugendubel
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The Next Level of Regionalism. Deep Integration...
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The Next Level of Regionalism. Deep Integration of Regio-Regio PTAs ab 44.99 EURO

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The Next Level of Regionalism. Deep Integration...
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The Next Level of Regionalism. Deep Integration of Regio-Regio PTAs ab 34.99 EURO

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Italo Gariboldi
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Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Italo Gariboldi (20 April 1879 - 3 February 1970) was a senior officer in the Italian Royal Army (Regio Esercito) before and during World War II.Gariboldi was born in Lodi, Lombardy.From the end of World War I and through the interwar Period, Gariboldi rose in the ranks and held various staff, regimental, and brigade level commands.In 1935, Gariboldi commanded the 30th Infantry Division "Sabauda" on the northern front during the Second Italo-Abyssinian War. His division was part of the I Corps based in Eritrea. After Italy defeated Ethiopia (Abyssinia) in 1936, Eritrea, Ethiopia, and Italian Somaliland were joined to form the colony of Italian East Africa.

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-Keto-Enones: Exploratory Studies on Their Phot...
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The result and discussion part of this book monitors a detailed in-depth mechanistic study with respect to the controlling effect of steric as well as electronic factors on photo-reactivity of mixed enones confined within semi cyclic framework. Proper justification in this area has been strongly supported by the exploratory research work exemplified by the author. In the review part of this book reader will also find a point to point discussion on photochemistry of enones, particularly in terms of alpha, bata- and beta, gamma-counterparts, in a very comprehensive manner starting from the very basic level to the advanced stage. Puckering of the geometry within this semi cyclic framework also becomes a constitutional factor to impose regio- as well as chemo-selectivity for the Wiitig reactions carried out on such kind of mixed enones. Content of the second chapter of this book has been purely focused on the effect of concentration on quantum yield. This typical uncommon effect has its selectiveness for a particular type of photo-product, the formation of which is very much dependent on the nature of the substitute pattern embedded with the substrate enone molecules.

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Synthetic pathway and process engineering for t...
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Biocatalysis shows high potential for the functionalization of unactivated C-H bonds at ambient conditions with absolute chemo-, regio-, and stereoselectivities being unrivalled by any chemical approach. In order to efficiently exploit nature’s toolbox towards an industrial implementation, engineering targets on the reaction as well as the catalyst level need to be identified and tackled in a concerted way.In this thesis, recombinant microbial cells containing the alkane monooxygenase AlkBGT from Pseudomonas putida GPo1 were applied for the w-functionalization of renewable fatty acid methyl esters (FAMEs). The resulting bifunctional products serve as building blocks for polymer syntheses. AlkBGT-containing Escherichia coli were shown to convert FAMEs with 5 to 12 carbon atoms in the alkyl chain giving the highest oxyfunctionalization activities (104 U gCDW -1 ) for nonanoic acid methyl ester. Kinetic studies revealed that AlkBGT catalyzes a three-step oxidation, yielding ?-alcohols, aldehydes and acids as products. In order to achieve ?-amino-functionalization, AlkBGT-based aldehyde formation was successfully coupled in recombinant E. coli with ?-transaminase catalysis (CV2025 from Chromobacterium violaceum), enabling the conversion of dodecanoic acid methyl ester (DAME) to 12-aminododecanoic acid methyl ester. Substrate uptake was identified as key factor limiting the conversion of the large and hydrophobic substrate DAME (1.4 U gCDW -1, 0.1 g L -1 h -1 ). Co-expression of the gene encoding the outer membrane protein AlkL relieved the uptake limitation and boosted the activities 62-fold to 87 U gCDW -1 allowing productivities of 4-8 g L -1 h -1 in two-liquid phase biotransformations. Furthermore, the latter reaction engineering concept enabled to control and govern product formation during AlkBGT-based multistep whole-cell biocatalysis. Overoxidation was prevented providing excess of substrate, yielding ?-alcohol as predominant product (up to 52 mM), whereas pronounced substrate limitation using bis(2-ethylhexyl)phthalate as organic carrier solvent resulted in almost exclusive acid accumulation (up to 93 mM). Introduction of the NAD(P)H-independent alcohol dehydrogenase AlkJ, which was shown to catalyze irreversible alcohol oxidation, into E. coli containing AlkBGT and AlkL enabled a shift towards the formation of overoxidized compounds in two-liquid phase biotransformations of DAME. This allowed the formation of the aldehyde as predominant product (up to 20 mM).Via catalyst and reaction engineering, this study sets the stage for the industrial implementation of recombinant microbial cells for terminal FAME functionalizations.

Anbieter: Dodax
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D-Keto-Enones: Exploratory Studies on Their Pho...
130,00 CHF *
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The result and discussion part of this book monitors a detailed in-depth mechanistic study with respect to the controlling effect of steric as well as electronic factors on photo-reactivity of mixed enones confined within semi cyclic framework. Proper justification in this area has been strongly supported by the exploratory research work exemplified by the author. In the review part of this book reader will also find a point to point discussion on photochemistry of enones, particularly in terms of alpha, bata- and beta, gamma-counterparts, in a very comprehensive manner starting from the very basic level to the advanced stage. Puckering of the geometry within this semi cyclic framework also becomes a constitutional factor to impose regio- as well as chemo-selectivity for the Wiitig reactions carried out on such kind of mixed enones. Content of the second chapter of this book has been purely focused on the effect of concentration on quantum yield. This typical uncommon effect has its selectiveness for a particular type of photo-product, the formation of which is very much dependent on the nature of the substitute pattern embedded with the substrate enone molecules.

Anbieter: Orell Fuessli CH
Stand: 15.08.2020
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