Bibliografías temáticas / Lanzhou Shi

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Literatura académica sobre el tema "Lanzhou Shi"

Autor: Grafiati
Publicado: 26 de julio de 2024
Última modificación: 31 de julio de 2025

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Artículos de revistas sobre el tema "Lanzhou Shi"

1

Wang, Yingying, Gang Cheng, Gouqin Wang, Xiaochun Zhou, Min Ma, and Jianqin Wang. "Predictive and diagnostic value of MCP-1, MIF, and ICAM-1 in Type-2 diabetes mellitus patients with diabetic kidney disease." Pakistan Journal of Medical Sciences 41, no. 7 (2025): 1943–48. https://doi.org/10.12669/pjms.41.7.12283.

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Objective: To explore the predictive value of monocyte chemoattractant protein-1 (MCP-1), macrophage migration inhibitory factor (MIF), and intercellular adhesion molecule-1 (ICAM-1) in patients with Type-2 diabetes mellitus (T2DM) complicated by diabetic kidney disease (DKD). Methods: This cross-sectional retrospective study included T2DN patients admitted to the Nephrology Department of Lanzhou University Second Hospital from September, 2022 to March, 2024. DKD was assessed by measuring the ratio of urinary albumin to creatinine. A Receiver Operating Characteristic (ROC) analysis was perform
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2

Yuan, Yamin, Yanfei Meng, Yihui Li, et al. "Development and validation of a nomogram for predicting 28-day in-hospital mortality in sepsis patients based on an optimized APACHE II score." Shock, February 5, 2024. http://dx.doi.org/10.1097/shk.0000000000002335.

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ABSTRACT Purpose The objective of this study is to establish a nomogram that correlates optimized APACHE II score with sepsis-related indicators, aiming to provide a robust model for early prediction of sepsis prognosis in clinical practice and serve as a valuable reference for improved diagnosis and treatment strategies. Methods This retrospective study extracted sepsis patients meeting the inclusion criteria from the MIMIC-IV database to form the training group. An optimized Acute Physiology and Chronic Health Evaluation (APACHE) II score integrated with relevant indicators was developed usi
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3

Kuang, Lanlan. "Staging the Silk Road Journey Abroad: The Case of Dunhuang Performative Arts." M/C Journal 19, no. 5 (2016). http://dx.doi.org/10.5204/mcj.1155.

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The curtain rose. The howling of desert wind filled the performance hall in the Shanghai Grand Theatre. Into the center stage, where a scenic construction of a mountain cliff and a desert landscape was dimly lit, entered the character of the Daoist priest Wang Yuanlu (1849–1931), performed by Chen Yizong. Dressed in a worn and dusty outfit of dark blue cotton, characteristic of Daoist priests, Wang began to sweep the floor. After a few moments, he discovered a hidden chambre sealed inside one of the rock sanctuaries carved into the cliff.Signaled by the quick, crystalline, stirring wave of sou
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4

Zhang, Zikun, Wanxia Zhang, Zhian Kou, et al. "First Report of Powdery Mildew Caused by Erysiphe polygoni on Trifolium repens in China." Plant Disease, May 10, 2022. http://dx.doi.org/10.1094/pdis-02-22-0289-pdn.

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White clover (Trifolium repens L.) belongs to the Fabaceae family legume and is cultivated in China for its medicinal properties and ornamental value. White clover is grown around the world for forage, turf , green manure and soil conservation purposes (Zhang el al. 2016). In October 2021, an investigation of a 1,000 m2 plant nursery in Lanzhou, China (36°06′N, 103°83′E) found that 80% of White clover plants were infected, and powdery mildew covered 95% of the leaf area. The disease had seriously destroyed the forage quality and reduced the ornamental value. Initially, thin, radial, irregular
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Libros sobre el tema "Lanzhou Shi"

1

Yang, Zhongqi. Lanzhou jing ji shi. Lanzhou da xue chu ban she, 1991.

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2

Lanzhou Shi Qilihe Qu di fang zhi bian zuan wei yuan hui., ed. Lanzhou Shi Qilihe Qu zhi. Gansu ren min chu ban she, 2001.

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3

Jinliang, Zhang, ed. Lanzhou li shi wen hua. Gansu ren min, 2007.

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4

Tonghe, Qian, ed. Lanzhou cheng guan shi hua. Gansu wen hua chu ban she, 2008.

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5

Tonghe, Qian, ed. Lanzhou cheng guan shi hua. Gansu wen hua chu ban she, 2008.

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6

Zhang, Kefei. Lanzhou da xue xiao shi: Lanzhoudaxuexiaoshi. Lanzhou da xue chu ban she, 2009.

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Lanzhou Shi di fang zhi bian zuan wei yuan hui . Lanzhou Shi zhi: Gong hui zhi. Lanzhou da xue chu ban she, 2010.

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8

Lanzhou Shi si fa xing zheng zh" bian wei hui. Lanzhou Shi si fa xing zheng zhi. Lanzhou da xue chu ban she, 1994.

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9

Lanzhou Shi Anning Qu Diaochang Xiang zhi bian zuan wei yuan hui. Lanzhou Shi Anning Qu Diaochang Xiang zhi. Lanzhou Shi Anning Qu Diaochang Xiang zhi bian zuan wei yuan hui, 2003.

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10

Lanzhou Jiaotong da xue xiao shi bian zhuan zu. Lanzhou Jiaotong da xue xiao shi, 1958--2008. Lanzhou Jiaotong da xue, 2008.

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Capítulos de libros sobre el tema "Lanzhou Shi"

1

Taber, Douglass F. "Other Methods for C–C Ring Construction: Pinolinone (Bach), Agelastatin A (Batey), Panaginsene (Lee), Salvileucalin D, Salvileucalin C (Ding), ent-Codeine (Hudlicky), Walsucochin B (Xie/Shi)." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0081.

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Thorsten Bach of the Technische Universität München used (Chem. Commun. 2014, 50, 3353) the chiral medium-mediated photochemical 2+2 cycloaddition that he devel­oped to prepare 3 by combining 1 with 2. Oxidative cleavage led to (−)-pinolinone 4. Robert A. Batey of the University of Toronto rearranged (Angew. Chem. Int. Ed. 2013, 52, 10862) furfural 5 in the presence of 6 to give the enone 7. Acylation fol­lowed by intramolecular conjugate addition delivered agelastatin A 8. Hee-Yoon Lee of KAIST prepared (Org. Lett. 2014, 16, 2466) the tosylhydrazone Na salt 9 from citronellal. Thermolysis led
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2

Taber, Douglass F. "C–H Functionalization: The Snyder Synthesis of (+)-Scholarisine A." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0020.

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Thomas R. Hoye of the University of Minnesota devised (Nature 2013, 501, 531) the reagent 2, that cyclized to a benzyne that in turn dehydrogenated the alkane 1 to the alkene 3, and 4. Abigail G. Doyle of Princeton University developed (J. Am. Chem. Soc. 2013, 135, 12990) a reagent combination for the allylic fluorination of a terminal alkene 5 to the branched product 6. Yan Zhang and Jianbo Wang of Peking University oxidized (Angew. Chem. Int. Ed. 2013, 52, 10573) the methyl group of 7 to give the nitrile 8. Hanmin Huang of the Lanzhou Institute of Chemical Physics found (Org. Lett. 2013, 15,
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3

Taber, Douglass F. "Organocatalytic C–C Ring Construction: Prostaglandin F2α (Aggarwal)." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0072.

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Marco Lombardo of the Università degli Studi di Bologna devised (Adv. Synth. Catal. 2012, 354, 3428) a silyl-bridged hydroxyproline catalyst that mediated the enantioselective addition of 2 to cinnamaldehyde 1 to give 3. Yoann Coquerel and Jean Rodriguez of Aix Marseille Université showed (Adv. Synth. Catal. 2012, 354, 3523) that a hybrid epi-cinchonine catalyst directed the enantioselective and diastereoselective addition of the amide 4 to the nitro alkene 5 to give 6. Magnus Rueping of RWTH Aachen observed (Angew. Chem. Int. Ed. 2012, 51, 12864) that a chiral Brønsted acid mediated the diast
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4

Taber, Douglass F. "C–N Ring Construction: The Harrity Synthesis of Quinolizidine (–)-217A." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0054.

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David M. Jenkins of the University of Tennessee devised (J. Am. Chem. Soc. 2011, 133, 19342) an iron catalyst for the aziridination of an alkene 1 with an aryl azide 2. Yoshiji Takemoto of Kyoto University cyclized (Org. Lett. 2011, 13, 6374) the prochiral oxime derivative 4 to the azirine 5 in high ee. Organometallics added to 5 syn to the pendant ester. Hyeung-geun Park of Seoul National University used (Adv. Synth. Catal. 2011, 353, 3313) a chiral phase transfer catalyst to effect the enantioselective alkylation of 6 to 7. Yian Shi of Colorado State University showed (Org. Lett. 2011, 13, 6
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5

Taber, Douglass F. "Functional Group Transformations." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0003.

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Mark Gandelman of the Technion–Israel Institute of Technology devised (Adv. Synth. Catal. 2011, 353, 1438) a protocol for the decarboxylative conversion of an acid 1 to the iodide 3. Doug E. Frantz of the University of Texas, San Antonio effected (Angew. Chem. Int. Ed. 2011, 50, 6128) conversion of a β-keto ester 4 to the diene 5 by way of the vinyl triflate. Pei Nian Liu of the East China University of Science and Technology and Chak Po Lau of the Hong Kong Polytechnic University (Adv. Synth. Catal. 2011, 353, 275) and Robert G. Bergman and Kenneth N. Raymond of the University of California,
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6

Lambert, Tristan H. "Reactions Involving Carbon–Carbon Bond Cleavage." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0028.

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Although they have historically played a relatively lesser role in organic synthesis, the appearance of a number of interesting methods that utilize C–C bond cleavage has prompted coverage in this chapter. Christopher W. Bielawski at the University of Texas at Austin found (Chem. Sci. 2012, 3, 2986) that the diamidocarbene 1 inserted into the C(O)–C(O) bond of dione 2 to produce 3 at room temperature. The use of oxalate monoester 5 for the decarboxylative cross-coupling with pyridine 4 to produce 6 was reported (Tetrahedron Lett. 2012, 53, 5796) by Yi-Si Feng at Hefei University of Technology.
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7

Taber, Douglass F. "C-O Ring Construction: (-)-Sclerophytin A (Morken), (+)-Dictyosphaeric Acid (Taylor), Goniothalesdiol A (Xie/She), (-)-7-Deoxyloganin (Lupton), (-)-Apicularen A (Uenishi), L-783, 277(Banwell) 100." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0052.

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In the course of a synthesis of (-)-sclerophytin A 3, James P. Morken of Boston College showed (J. Am. Chem. Soc. 2010, 132, 16380) that Oshima-Utimoto conditions transformed 1 into 2 with high stereo-and regiocontrol. En route to (+)-dictyosphaeric acid 6, Richard J. K. Taylor of the University of York found (Angew. Chem. Int. Ed. 2010, 49, 5574) that the intramolecular Michael cyclization of 4 proceeded smooothly to give 5. Xingang Xie and Xuegong She of Lanzhou University devised (Synlett 2010, 2283) the In-mediated cyclization of 7 with benzaldehyde, to effect an elegant synthesis of gonio
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8

Taber, Douglass F. "C–O Ring Construction: Sauropus Hexoside (Xie/Wu), (+)-Ipomeamarone (Usuki), Decytospolide A (Fujioka), Cytospolide P (Goswami), (+)-Didemniserinolipid B (Tong), Gymnothelignan N (She)." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0051.

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A range of biological activity was observed for the group of 3,6-anhydro-2-deoxy hexosides, of which 3 is representative, isolated from Sauropus rostratus. Wei-Jia Xie and Xiao-Ming Wu of China Pharmaceutical University prepared (Org. Lett. 2014, 16, 5004) 3 by the dealkylative cyclization of 1 to 2. (+)-Ipomeamarone 6 is a phytoalexin isolated from mold-damaged sweet pota­toes. Yoshinosuke Usuki of Osaka City University assembled (Chem. Lett. 2014, 43, 1882) 6 by the diastereoselective cyclization of 4 to 5. Hiromichi Fujioka of Osaka University protected (Org. Lett. 2014, 16, 3680) the enone
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9

Taber, Douglass F. "Alkaloid Synthesis: (–)-α-Kainic Acid (Cohen), Hyacinthacine A2 (Fox), (–)-Agelastatin A (Hamada), (+)-Luciduline (Barbe), (+)-Lunarine (Fan), (–)-Runanine (Herzon)." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0058.

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The intramolecular ene cyclization is still little used in organic synthesis. Theodore Cohen of the University of Pittsburgh trapped (J. Org. Chem. 2011, 76, 7912) the cyclization product from 1 with iodine to give 2, setting the stage for an enantiospecific total synthesis of (–)-α-kainic acid 3. Intramolecular alkene hydroamination has been effected with transition metal catalysts. Joseph M. Fox of the University of Delaware isomerized (Chem. Sci. 2011, 2, 2162) 4 to the trans cyclooctene 5 with high diastereocontrol. Deprotection of the amine led to spontaneous cyclization, again with high
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10

Taber, Douglass F. "Enantioselective Synthesis of Alkylated Centers: The Fukuyama Synthesis of (–)-Histrionicotoxin." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0039.

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Vinod K. Singh of the Indian Institute of Technology, Kanpur optimized (Org. Lett. 2011, 13, 6520) an organocatalyst for the enantioselective addition of thiophenol to an imide 1 to give 2 in high ee. Amir H. Hoveyda of Boston College developed (Angew. Chem. Int. Ed. 2011, 50, 7079) a Cu catalyst for the preparation of 4 by the enantioselective hydroboration of a 1,1-disubstituted alkene 3. Yong-Qiang Tu of Lanzhou University effected (Chem. Sci. 2011, 2, 1839) enantioselective bromination of the prochiral 5 to give the bromoketone 6. Song Ye of the Institute of Chemistry, Beijing established
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