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  • 1
    Monograph available for loan
    Monograph available for loan
    Flora Qinghaiica; Vol. 1 (1997)
    Xining : Qinghai People's Publ. House
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    Call number: AWI Bio-18-91553-1
    In: Flora Qinghaiica, Vol. 1
    Type of Medium: Monograph available for loan
    Pages: 544 Seiten , Illustrationen
    ISBN: 722501448x
    Language: Chinese , Latin
    Note: Contents: Selaginellaceae, Equisetaceae, Pteridaceae, Sinopteridaceae, Adiataceae, Hemionidaceae, Athyriaceae, Aspleniaceae, Onocleaceae, Woodsiaceae, Dryopteridaceae, Polypodiaceae, Drynariaceae, Pinaceae, Cupressaceae, Ephedraceae, Utricaceae / Mei Li-juan. - Salicaceae / Ding Tuo-ya. - Juglandaceae, Betulaceae, Fagaceae, Ulmaceae, Moraceae, Santalaceae, Loranthaceae, Polygonaceae, Chenopodiaceae, Amaranthaceae, Cruciferae / Huang Rong-fu. - Caryophyllaceae, Ranunculaceae, Berberidaceae, Lauraceae, Papaveraceae / Zhou Li-hua. - Delineatores / Wang Ying, Yan Cui-lan, Liu Jin-jun, Zhang Gui-zhi, Feng Jin-huan, Zhou Qing-jun. , In chines. Schr. - Nomenklatur in lat. Schr.
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  • 2
    Monograph available for loan
    Monograph available for loan
    Flora Reipublicae Popularis Sinicae; Tomus 26, Angiospermae : Dicotyledonae ; Nyctaginaceae, Phytolaccaceae, Aizoaceae, Portulacaceae, Basellaceae, Caryophyllaceae (1996)
    Beijing : Science Press
    Associated volumes
    Details Availability
    Call number: AWI Bio-18-91599-26
    In: Flora Reipublicae Popularis Sinicae, Tomus 26
    Type of Medium: Monograph available for loan
    Pages: 506 Seiten , Illustrationen
    ISBN: 7030048873
    Language: Chinese , Latin
    Note: Table of Contents: NYCTAGINACEAE. - 1. Pisonia L. - 1. P. aculeata L.. - 2. Ceodes J. et G. Forst. - 1. C. grandis (R. Br.) D. Q. Lu. - 2. C. umbellifera J. et G. Forst. - 3. Bougainvillea Comm. ex Juss. - 1. B. glabra Choisy. - 2. spectabilis Willd. - 4. Mirabilis L. - 1. M. jalapa L. - 5. Oxybaphus L' Her. ex Willd. - 1. O. himalaicus Edgew. - 6. Boerhavia L. - 1. B. diffusa L. - 2. B. erecta L.. - 3. B. crispa Heyne. - 7. Commicarpus Standl. - 1. C. chinensis (L. ) Heim. - 2. C. lantsangensis D. Q. Lu. - PHYTOLACCACEAE. - 1. Phytolacca L. - 1. Ph. acinosa Roxb. - 2. Ph. polyandra Batalin. - 3. Ph. japonica Makino. - 4. Ph. americana L. - 2. Rivina L. - 1. R. humilis L. - AIZOACEAE. - 1. Gisekia L. - 1. G. pharnaceoides L. - 2. Glinus L. - 1. Gl. lotoides L. - 2. Gl. oppositifolius (L.) A. DC. - 3. Mollugo L. - 1. M. nudicaulis Lam. - 2. M. cerviana (L.) Ser. - 3. M. stricta L. - 4. M. verticillata L. - 4. Sesuvium L. - 1. S. portulacastrum (L.) L. - 5. Trianthema L. - 1. Tr. portulacastrum L. - 6. Mesembryanthemum L. - 1. M. cordifolium L. f. - 2. M. crystallinum L. - 3. M. uncatum Salm-Dyck. - 4. M. edule L.. - 5. M. spectabile Haw. - 7. Tetragonia L. - 1. T . tetragonioides (Pall. ) Kuntze. - PORTULACACEAE. - 1. Portulaca L. - 1. P. oleracea L. - 2. P. pilosa L. - 3. P. grandiflora Hook - 4. P. quadrifida L. - 5. P. psammotropha Hance. - 6. P. insularis Hosokawa. - 2. Talinum Adans. - 1. T. paniculatum (Jacq.) Gaertn. - BASELLACEAE. - 1. Basella L. - 1. B. alba L. - 2. Anredera Juss. - 1. A. scandens (L.) Moq. - 2. A. cordifolia (Tenore) Steenis. - CARYOPHYLLACEAE. - I. Subfam. PARONYCHIOIDEAE Vierh. - 1. Trib. PARONYCHIEAE Pax. - 1. Gymnocarpos Forssk. - 1. G. przewalskii Maxim. - 2. Herniaria L. - 1. H. glabra L. - 2. H. polygama J. Gay. - 3. H. caucasica Rupr. - 2. Trib. SPERGULEAE Vierh. - 3. Spergula L. - 1. Sp. arvensis L. - 4. Spergularia (Pers.) J. et C. Presl. - 1. Sp. rubra (L.) J. et C. Presl. - 2. Sp. diandra (Guss.) Heldr. et Sart. - 3. Sp. media (L.) C. Presl. - 4. Sp. salina J. et C. Presl. - 3. Trib. POLYCARPEAE Pax. - 5. Drymaria Willd. ex Roem. et Schult. - 1. Dr. villosa Cham. et Schlecht. - 2. Dr. diandra Bl. - 6. Polycarpon Loefl. ex L. - 1. P. prostratum (Forssk.) Aschers. et Schweinw. - 7. Polycarpaea Lam. - 1. P. corymbosa (L.) Lam. - 2. P. gaudichaudii Gagnep. - ll. Subfam. ALSINOIDEAE Vierh. - 1. Subtrib. STELLARIINAE Aschers. et Graebn. - 8. Pseudostellaria Pax. - 1. Ps. sylvatica (Maxim.) Pax. - 2. Ps. heterophylla (Miq.) Pax. - 3. Ps. japonica (Korsh.) Pax. - 4. Ps. davidii (Franch.) Pax. - 5. Ps. rupestris (Turcz.) Pax. - 6. Ps. heterantha (Maxim.) Pax. - 7. Ps. himalaica (Franch.) Pax. - 8. Ps. maximowicziana (Franch. et Sav.) Pax. - 9. Myosoton Moench. - 1. M. aquaticum (L.) Moench. - 10. Cerastium L. - 1. C. cerastoides (L.) Britt. - 2. C. pauciflorum Stev. ex Ser. - 3. C. falcatum Bge. - 4. C. maximum L. - 5. C. lithospermifolium Fisch. - 6. C. dahuricum Fisch. - 7. C. perfoliaturn L. - 8. C. glomeratum Thuill. - 9. C. furcatum Cham. et Schlecht. - 10. C. fontanum Baumg. - 11. C. tianschanicum Schischk. - 12. C. limprichtii Pax et Hoffm. - 13. C. szechuense Williams. - 14. C. wilsonii Takeda. - 15. C. pusillum Ser. - 16. C. baischanense Y. C. Chu. - 17. C. arvense L. - 18. C. subpilosum Hayata. - 11. Stellaria L. - 1. Sect. Stellaria. - 1. Subsect. Stellaria. - 1. Ser. Petiolares Fenzl. - 1. St. bungeana Fenzl. - 2. St. nemorum L. - 3. St. nepalensis Majumdar et Vartak. - 4. St. arisanensis (Hayata) Hayata. - 5. St. wushanensis Williams. - 6. St. neglecta Weihe ex Bluff et Fingerh. - 7. St. media (L.) Cyr. - 8. St. apetala Ucria ex Roem. - 9. St. vestita Kurz. - 10. St. chinensis Regel. - 11. St. pilosa Franch. - 12. St. petiolaris Hand. -Mazz. - 13. St. lanipes C. Y. Wu et H. Chuang. - 2. Ser. Sessilifoliae Y. W. Tsui ex P. Ke. - 14. St. omeiensis C. Y. Wu et Y. W. Tsui ex P. Ke. - 15. St. reticulivena Hayata. - 16. St. infracta Maxim. - 17. St. gyirongensis L. H. Zhou. - 18. St. zangnanensis L. H. Zhou. - 19. St. tibetica Kurz. - 20. St. lanata Hook. f. ex Edgew. et Hook. f. - 21. St. patens D. Don. - 3. Ser. Dichotomae Roshev. - 22. St. dichotoma L. - 23. St. amblyosepala Schrenk. - 4. Ser. Holosteae Fenzl. - 24. St. henryi Williams. - 2. Subsect. Larbraea (St. Hil.) Fenzl. - 1. Ser. Foliaceo-bracteatae Schischk. - 25. St. ebracteata Korn. - 26. St. winkleri (Briq.) Schischk. - 27. St. crassifolia Ehrh. - 2. Ser. Discolares Schischk. - 28. St. discolor Turcz. - 29. St. gyangtseensis Williams. - 3. Ser. Uliginosae Schischk. - 30. St. pusilla E. Schmid. - 31. St. mainlingensis L. H. Zhou. - 32. St. depressa E. Schmid. - 33. St. uliginosa Murr. - 4. Ser. Gramineae Roshev. - 34. St. graminea L. - 35. St. brachypetala Bge. - 36. St. yunnanensis Franch. - 37. St. palustris Ehrh. ex Retz. - 38. St. salicifolia Y. W. Tsui ex P. Ke. - 39. St. dianthifolia Williams. - 40. St. longifolia Muehl. ex Willd. - 41. St. imbricata Bge. - 42. St. nipponica Ohwi. - 43. St. filicaulis Makino. - 5. Ser. Parviflorae Schischk. - 44. St. alaschanica Y. Z. Zhao. - 45. St. oxycoccoides Korn. - 46. St. uda Williams. - 47. St. souliei Williams. - 6. Ser. Pedunculares Schischk. - 48. St. soongorica Roshev. - 7. Ser. Umbellatae Schischk. - 49. St. irrigua Bge. - 50. St. parvi-umbellata Y. Z. Zhao. - 51. St. umbellata Turcz. - 52. St. suburnbellata Edgew.. - 2. Sect. Adenonerna (Bge.) Pax. - 53. St. arenaria Maxim.. - 54. St. cherleriae (Fisch. ex Ser.) Williams. - 55. St. petraea Bge. - 56. St. decumbens Edgew. - 57. St. congestiflora Hara. - 3. Sect. Fimbripetalurn Turcz. - 58. St. radians L. - 4. Sect. Leucostemma (Benth. ex G. Don f.) Pax. - 59. St. rnartjanovii Krylov. - 5. Sect. Schizothecium Fenzl. - 60. St. monosperma Buch. -Ham. ex D. Don. - 61. St. ovatifolia (Mizushima) Mizushima. - 62. St. delavayi Franch. - 6. Sect. Oligosperma Boiss. - 63. St. bistyla Y. Z. Zhao. - 64. St. strongylosepala Hand.-Mazz. - 12. Holosteum L. - 1. H. umbellatum L. - 13. Arenaria L. - 1. Subgen. Arenaria. - 1. Sect. Arenaria. - 1. A. serpyllifolia L. - 2. Sect. Rotundifoliae McNeill. - 2. A. orbiculata Royle ex. Edgew. et Hook f. - 3. A. neelgerrensis Wight et Arn. - 3. Sect. Rariflorae Williams. - 4. A. monosperma Williams. - 5. A. puranensis L. H. Zhou. - 4. Sect. Compressae McNeill. - 6. A. compressa McNeill. - 2. Subgen. Eremogone (Fenzl) Fenzl. - 1. Sect. Monogone Maxim. - 7. A. potaninii Schischk. - 2. Sect. Capillares McNeill. - 8. A. juncea M. Bieb. - 9. A. capillaris Poir. - 10. A. acicularis Williams ex Keissler. - 11. A. grüningiana Pax et Hoffm. - 12. A. formosa Fisch. ex Ser. - 13. A. haitzeshanensis Y. W. Tsui. - 3. Sect. Sclerophyllae (Boiss.) McNeill. - 14. A. griffithii Boiss. - 15. A. androsacea Grub. - 3. Subgen. Eremogoneastrum Williams. - 16. A. brevipetala Y. W. Tsui et L. H. Zhou. - 17. A. baxoiensis L. H. Zhou. - 18. A. kumaonensis Maxim. - 19. A. kansuensis Maxim. - 20. A. ischnophylla Williams. - 21. A. roborowskii Maxim. - 22. A. lancangensis L. H. Zhou. - 23. A. gerzeensis L. H. Zhou. - 24. A. qinghaiensis Y. W. Tsui et L. H. Zhou. - 25. A. aksayqingensis L. H. Zhou. - 26. A. pulvinata Edgew. - 27. A. shannanensis L. H. Zhou. - 28. A. edgeworthiana Majumdar. - 29. A. bryophylla Fernald. - 30. A. zadoiensis L. H. Zhou. - 31. A. taibaishanensis L. H. Zhou. - 32. A. festucoides Benth. - 4. Subgen. Dolophragma (Fenzl) McNeill. - 33. A. przewalskii Maxim. - 34. A. smithiana Mattf. - 35. A. oreophila Hook. f. ex Edgew. et Hook. f. - 36. A. densissima Wall. ex Edgew. et Hook. f. - 37. A. polytrichoides Edgew. ex. Edgew. et Hook f. - 5. Subgen. Solitaria McNeill. - 38. A. ciliolata Edgew. - 39. A. ramellata Williams. - 40. A. stracheyi Edgew. - 41. A. rhodantha Pax et Ho , Text in chinesischer Schrift , Überschriften in lateinischer Sprache
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  • 3
    Electronic Resource
    Electronic Resource
    Effect of Er〈sup〉3+〈/sup〉 Doping on Crystallization of PbF〈sub〉2〈/sub〉-SiO〈sub〉2〈/sub〉 Based Bulk Xerogels (2007)
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 336-338 (Apr. 2007), p. 2322-2324 
    Details
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Transparent glass ceramics with composition of xErF3-10PbF2-90SiO2 (mol%, x=0, 1, 2, 3, 4)were prepared by sol-gel method. The thermal behavior of the xerogels was investigated by DSC.Through non-isothermal experiments, the apparent activation energy for the crystallization of β-PbF2phase was evaluated by the Kissinger’s method and Chen’s method. XRD and TEM were carried out tostudy the growth of β-PbF2 nanocrystals and the effect of Er3+ doping on it
    Type of Medium: Electronic Resource
    URL: http://www.tib-hannover.de/fulltexts/2011/0528/01/53/transtech_doi~10.4028%252Fwww.scientific.net%252FKEM.336-338.2322.pdf
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  • 4
    Electronic Resource
    Electronic Resource
    Synthesis of Nanocrystalline Ce〈sub〉0.8〈/sub〉Sm〈sub〉0.2〈/sub〉O〈sub〉1.9〈/sub〉 by Citrate Gel Method (2008)
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 368-372 (Feb. 2008), p. 247-249 
    Details
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A citrate gel method was applied to synthesize Ce0.8Sm0.2O1.9 powders by using cerium andsamarium nitrates as raw materials and citric acid as complexing agent. It was shown that Ce0.8Sm0.2O1.9phase was formed when the decomposition of the dried gel completed at 500 °C. The crystallite size of thesynthesized powders calcined at 500 °C for 2 h is 5-10 nm. The powders can be easily sintered in air toyield over 97 % relative density at 1250 °C, which is significantly lower than sintering temperature ofover 1500°C required by the doped ceria powders prepared via conventional ceramic techniques
    Type of Medium: Electronic Resource
    URL: http://www.tib-hannover.de/fulltexts/2011/0528/01/56/transtech_doi~10.4028%252Fwww.scientific.net%252FKEM.368-372.247.pdf
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  • 5
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    Theoretical study on the mechanisms of Proline-catalyzed Mannich reaction between acetaldehyde and N-Boc imines (2012)
    Wiley
    Details
    Publication Date: 2012-04-15
    Description: The mechanisms of the single and double Mannich reactions between acetaldehyde and N-Boc imines are clarified by density functional theory calculations. For single addition of Mannich reaction, the energy difference between the transition states of different configurations correspond to an enantiomeric excess value of 90.58% (without solvent) and 98.46% (in acetonitrile) in favor of the (S)-configuration product. For bis-addition of Mannich reaction, the calculated enantiomeric excess value is 95.02% (without solvent) and 98.57% (in acetonitrile) in favor of the (S, S)-configuration product. These calculated results are in good agreement with the experimental results. The calculations clearly demonstrate that the hydrogen-bonding determine the stereochemistry of the reactions. Copyright © 2012 John Wiley & Sons, Ltd. DFT calculations demonstrate that the single and double Mannich reactions between acetaldehyde and N-Boc imines lead to the formation of the (S)-configuration and (S, S)-configuration products, respectively; the hydrogen-bonding determine the stereochemistry of the reactions and the solvent employed play an important role in determining the reaction rate and enantioselectivity.
    Print ISSN: 0894-3230
    Electronic ISSN: 1099-1395
    Topics: Chemistry and Pharmacology , Physics
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  • 6
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    Propofol Protects Against H2O2-Induced Oxidative Injury in Differentiated PC12 Cells via Inhibition of Ca2+-Dependent NADPH Oxidase (2015)
    Springer
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    Publication Date: 2015-07-11
    Print ISSN: 0272-4340
    Electronic ISSN: 1573-6830
    Topics: Biology
    Published by Springer
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  • 7
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    Semismooth Newton support vector machine (2007)
    Elsevier
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    Publication Date: 2007-11-01
    Print ISSN: 0167-8655
    Electronic ISSN: 1872-7344
    Topics: Computer Science
    Published by Elsevier
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  • 8
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    Theoretical study on the mechanisms of Proline-catalyzed Mannich reaction between acetaldehyde and N-Boc imines (2012)
    Wiley
    Details
    Publication Date: 2012-01-11
    Description: The mechanisms of the single and double Mannich reactions between acetaldehyde and N-Boc imines are clarified by density functional theory calculations. For single addition of Mannich reaction, the energy difference between the transition states of different configurations correspond to an enantiomeric excess value of 90.58% (without solvent) and 98.46% (in acetonitrile) in favor of the (S)-configuration product. For bis-addition of Mannich reaction, the calculated enantiomeric excess value is 95.02% (without solvent) and 98.57% (in acetonitrile) in favor of the (S, S)-configuration product. These calculated results are in good agreement with the experimental results. The calculations clearly demonstrate that the hydrogen-bonding determine the stereochemistry of the reactions. Copyright © 2012 John Wiley & Sons, Ltd. DFT calculations demonstrate that the single and double Mannich reactions between acetaldehyde and N-Boc imines lead to the formation of the (S)-configuration and (S, S)-configuration products, respectively; the hydrogen-bonding determine the stereochemistry of the reactions and the solvent employed play an important role in determining the reaction rate and enantioselectivity.
    Print ISSN: 0894-3230
    Electronic ISSN: 1099-1395
    Topics: Chemistry and Pharmacology , Physics
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  • 9
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    Discovery and Characterization of the Highly Active Fungal Immunomodulatory Protein Fip-vvo82 (2016)
    American Chemical Society (ACS)
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    Publication Date: 2016-09-30
    Description: Journal of Chemical Information and Modeling DOI: 10.1021/acs.jcim.6b00087
    Topics: Chemistry and Pharmacology
    Published by American Chemical Society (ACS)
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  • 10
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    Mixed-solvothermal synthesis of hybrid nanostructures of alkaline earth phenylphosphonates (2007)
    Elsevier
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    Publication Date: 2007-11-01
    Print ISSN: 0167-577X
    Electronic ISSN: 1873-4979
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Published by Elsevier
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