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  • Wiley-Blackwell  (49)
  • 1980-1984  (49)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 29 (1983), S. 903-909 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A unified approach is proposed for the prediction of heat transfer coefficients in turbulent falling films undergoing heating, evaporation or condensation for both of the cases with or without interfacial shear. A modified van Driest eddy viscosity model, which incorporated a damping factor f and takes into account the effect of variable shear stress, is used to predict the hydrodynamics of turbulent falling films. The calculated film thicknesses are in good agreement with the Nusselt-Brauer correlations for the non-sheared film and the Dukler prediction for highly sheared film. Also, by including a van Driest type turbulent Prandtl number model, the asymptotic heat transfer coefficients are accurately predicted and show better agreement with the extensive literature data and correlations than do most of the existing turbulence models proposed to date.
    Additional Material: 10 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 3 (1983), S. 491-500 
    ISSN: 0886-1544
    Keywords: actin ; microfilaments ; oligomers ; transmembrane glycoprotein ; microvilli ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The organization of microvillus actin and its associated proteins have been investigated in sublines of mammary ascites tumors (MAT) with mobile (MAT-B1) and immobile (MAT-C1) cell surface receptors. Microvilli isolated from these sublines differ in morphology (branched for MAT-C1 versus unbranched for MAT-B1) and the presence of a 58,000-dalton polypeptide (58K). 58K is found associated with MAT-C1 microvilli, microvillar cytoskeletons obtained by nonionic detergent extractions, and microvillar membranes prepared under conditions which depolymerize actin microfilaments. By extraction with actin-stabilizing buffers (isotonic Triton-Mg-ATP) microvillar actin can be fractionated into four forms. About 40% of the actin is sedimented at low speed (7,500g, 15 min). The pellets contain microfilaments; actin and α-actinin are the predominant proteins. High-speed pellets from these low-speed supernates contain about 10% of the actin as a transmembrane complex with a cell surface glycoprotein (cytoskeleton-associated glycoprotein, [CAG] 75-80,000 daltons) in MAT-B1 cells or with CAG and 58K in MAT-C1 cells. Transmembrane complexes can be purified from MAT-B1 and MAT-C1 microvillar membranes in Triton-containing buffer by gel filtration or sucrose density gradient centrifugation. The presence of only CAG and actin in the MAT-B1 transmembrane complex strongly suggests the direct interaction of actin and a cell surface component. The high-speed supernates contain soluble actin. By gel filtration or rate-zonal sucrose density gradient centrifugation about 30% of the microvillar actin is found as small oligomers and about 10% as G-actin in this extraction buffer. We suggest that the actin-containing transmembrane complexes may serve as membrane-association sites for oligomeric actin segments and microfilaments and as initiation sites for actin polymerization.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1775-1789 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Stereospecific Synthesis of Nucleoside-5′-carboxylic Acid Derivatives with Pyrimidines as Hetero-cyclic BasePyrimidine nucleoside-5′-carboxylic acid derivatives were synthesized by condensation of riburonic acid glycosyl halides with heterocyclic bases via different methods. According to the investigations, the benzoyl-protected riburonic acid glycosyl halides 3b and 16b are valuable starting materials for the synthesis of β-nucleosides. Silver perchlorate proved to be the best catalyst in these condensation reactions with respect to stereoselectivity and yield. The methyl esters and the ethyl amides of uridine-, cytidine-, and thymidine-5′-carboxylic acid 8b, 11b, 18b, 19b and 20b were synthesized by this method stereospecifically and in good yield.
    Notes: Pyrimidinnucleosid-5′-carbonsäure-Derivate wurden durch Kondensation von Riburonsäure-glycosylhalogeniden mit heterocyclischen Basen nach verschiedenen Methoden hergestellt. Nach den Untersuchungen eignen sich als Ausgangskomponenten zur Synthese der β-Nucleoside am besten die benzoyl-geschützten Riburonsäure-glycosylhalogenide 3b und 16b. Die Verwendung von Silberperchlorat als Katalysator für die Kondensation ergab insgesamt die besten Ergebnisse bezüglich Stereoselektivität und Ausbeute. Die Methylester bzw. Ethylamide 8b, 11b, 18b, 19b und 20b der Uridin-, Cytidin- und Thymidin-5′-carbonsäure wurden auf diese Weise stereospezifisch und mit guten Ausbeuten synthetisiert.
    Additional Material: 2 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 740-745 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Acetals of L-Rhamnose with Lithium-organic Compounds New Syntheses of Mycaral, Olivomycal, and Methyl 2,3,6-Trideoxy-α-L-erythro-hex-2-enopyranosideMethyl α-L-mycaroside (6a) is obtained from the dideoxy-uloside 2) by Grignard addition. the benzylidene rhamnoside (1a) reacts with methyllithium to give in only one step mycaral (4) (21%) and olivomycal (5) (72%). With lithiumdiisopropylamide 1a yields the unsaturated sugar 3a.
    Notes: Methyl-α-L-mycarosid (6a) wird aus dem Didesoxy-ulosid 2 durch Grignard-Addition erhalten. Das Benzylidenrhamnosid 1a reagiert mit Methyllithium in einem schritt zu Mycaral (4) und Olivomycal (5). Mit Lithiumdiisopropylamid erhält man hingegen aus 1a den ungesättigten Zucker 3a.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1761-1767 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Acetals of L-Sorbose with n-Butyllithium2,3:4,6-Di-O-isopropylidene-α-L-sorbose (1a) gives with n-butyllithium the known 6-deoxy-2,3-O-isopropylidene-β-D-threo-hex-5-enulofuranose (2), while the corresponding benzylidene compound 4 yields the glycal derivative 2,5-anhydro-4,6-O-benzylidene-3-deoxy-L-threo-hex-2-enitol (5). The 1-benzyl ether 1b is converted into 3 by Wittig rearrangement. Under analogous conditions both possible Wittig rearrangement products 7a and b are obtained from methyl 6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranoside (6). Their configuration is established by 1H NMR spectroscopy.
    Notes: 2,3:4,6-Di-O-isopropyliden-α-L-sorbose (1a) ergibt mit n-Butyllithium die bekannte 6-Desoxy-2,3-O-isopropyliden-β-D-threo-hex-5-enulofuranose (2), während die entsprechende Benzylidenverbindung 4 das Glycal-Derivat 2,5-Anhydro-4,6-O-benzyliden-3-desoxy-L-threo-hex-2-enitol (5) liefert. Aus dem 1-Benzylether 1b entsteht u. a. durch Wittig-Umlagerung das Produkt 3. Unter den gleichen Bedingungen werden aus Methyl-6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosid (6) beide möglichen Wittig-Umlagerungsprodukte 7a und 7b erhalten. Ihre Konfigurationszuordnung erfolgt aus dem 1H-NMR-Spektrum.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 2834-2843 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Glycosylhydrazines, 5. Synthesis of pyrazole-, Pyrazolo[3,4-d]pyrimidine-, and 1H-1,2,4-Triazol-Nucleoside 5′-amide Derivatives via Riburonamide HydrazonesIn a single step reaction the 3,5-dimethylpyrazole nucleoside-5′-amides 6a,c, the functionally substituted pyrazole nucleoside-5′-amides 9a and 10b, and the 1H-1,2,4-triazol-nucleoside-5′-amide 18 were obtained regio- and stereoselectively from the riburonamide hydrazones 4a-c.9a and 10b were transformed into the unprotected pyrazolo[3,4-d]pyrimidine nucleoside-5-amide 14a and 15b, derivatives of allopurinol riboside. likewise the ethylamide 20 of virazole-5′-acid was synthesized from 18.
    Notes: Aus den Riburonamid-hydrazonen 4a-c wurden in einer Eintopfreaktion regio- und stereoselektiv die 5′-Säureamid-Derivate des 3,5-Dimethylpyrazol-nucleosids 6a,c, der funktionell substituierten Pyrazol-nucleoside 9a) und 10n) und des 1H-1,2,4-Triazole-nucleosids 18 direkt aufgebaut. Als Allopurinolribosid-Derivate wurden aus 9a und 10b die ungeschützten pyrazolo[3,4-d]pyrimidin-nucleosid-5′-säureamide 14a und 15b hergestellt. Entsprechend wurde aus 18 das Ethylamid 20, der Virazol-5′-säure erhalten.
    Additional Material: 1 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 804-807 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acetylenedicarbonyl DichlorideIn situ prepared carbonyl chloride 2 can be used as „activated acetylenedicarboxylic acid“ in Diels-Alder syntheses.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 1192-1195 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of Acetals of Sugars with Organolithium Compounds A Simple Synthesis of 4,6-Dideoxy-α-D-erythro-hexopyranos-3-ulose1,2:3,4-Di-O-isopropylidene-β-L-arabinose (3) reacts with lithium diisopropylamide to give the 4-deoxy-4-eno sugar 4. After its oxidation a stereospecific 1,4-addition by methyllithium/copper (I) iodide yields the 4,6-dideoxy-3-ulose 6.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1982 (1982), S. 1322-1329 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Konformation von Peptiden mit α-Aminoisobuttersäure.  -  Die Kristallstruktur von Boc-Gly-L-Ala-Aib-OMeBoc-Gly-L-Ala-Aib-OMe (1) kristallisiert in der Raumgruppe P212121 mit a = 10.043(3), b = 11.590(5), c = 16.779(1) Å und Z = 4 (R-Faktor für 1859 symmetrieunabhängige Reflexe: 0.043). Das Tripeptid bildet über eine 4 → 1-intramolekulare Wasserstoffbrückenbindung einen “β-turn”-Typ III, obwohl das Cα-Atom im Aib-Rest nicht direkt an dem “β-turn”-Ringsystem beteiligt ist. Intermolekulare Wasserstoffbrücken verknüpfen die Einzelmoleküle schraubenförmig entlang [100].
    Notes: Boc-Gly-L-Ala-Aib-OMe (1) crystallizes in the space group P212121 with a = 10.043(3), b = 11.590(5), c = 16.779(1) Å, and Z = 4 (R value for 1859 symmetry independent reflexions: 0.043). On the basis of a 4 → 1 intramolecular hydrogen bond, the tripeptide forms a β-turn type III, although the Cα atom in the Aib residue is not directly involved in the β-turn ring system. Inter-molecular hydrogen bonds link the single molecules to helical structures along [100].
    Additional Material: 3 Ill.
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  • 10
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Carbohydrate Acetals with Organolithium Compounds.  -  Synthesis of 3-Deoxy-α-D-erythro-hexofuranosid-2-ulose and 6-Deoxy-α-D-xylo-hexofuranos-5-uloseMethyl 2,3:5,6-di-O-isopropylidene-α-D-mannofuranoside (1) reacts with lithium diisopropylamide to give the methyl 3-deoxy-5,6-O-isopropylidene-α-D-erythro-hexofuranosid-2-ulose (2), while 1,2-O-isopropylidene-3,5,6-O-methylidyne-α-D-glucofuranose (3) yields 6-deoxy-1,2-O-isopropylidene-α-D-xylo-hexofuranos-5-ulose (4).
    Notes: Das Methyl-2,3:5,6-di-O-isopropyliden-α-D-mannofuranosid (1) reagiert mit Lithiumdiisopropylamid zur Methyl-3-desoxy-5,6-O-isopropyliden-α-D-erythro-hexofuranosid-2-ulose (2), während die 1,2-O-Isopropyliden-3,5,6-O-methylidin-α-D-glucofuranose (3) die 6-Desoxy-1,2-O-isopropyliden-α-D-xylo-hexofuranos-5-ulose (4) liefert.
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