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Статті в журналах з теми "Lead (II) compounds"
Jones, Jamie N., та Alan H. Cowley. "π-Indenyl tin(ii) and lead(ii) compounds". Chem. Commun., № 10 (2005): 1300–1302. http://dx.doi.org/10.1039/b410549d.
Повний текст джерелаWang, Yin, Yanjiao Xie, Wenlu Li, Zimeng Wang, and Daniel E. Giammar. "Formation of Lead(IV) Oxides from Lead(II) Compounds." Environmental Science & Technology 44, no. 23 (December 2010): 8950–56. http://dx.doi.org/10.1021/es102318z.
Повний текст джерелаHarrowfield, JM, H. Miyamae, BW Skelton, AA Soudi, and AH White. "Lewis-Base Adducts of Lead(II) Compounds. XVI. Synthetic and Structural Studies of Some Adducts of 2-Aminomethylpyridine With Lead(II) Compounds." Australian Journal of Chemistry 49, no. 10 (1996): 1127. http://dx.doi.org/10.1071/ch9961127.
Повний текст джерелаHan, Kyoung R., Hee Jin Koo, and Chang Sup Lim. "Novel Route to Lead-Based Ferroelectric Compounds via Tetragonal Lead(II) Oxide Intermediates." Journal of the American Ceramic Society 83, no. 9 (December 20, 2004): 2214–18. http://dx.doi.org/10.1111/j.1151-2916.2000.tb01537.x.
Повний текст джерелаBowes, Scott, Dongyu Sun, Azita Kaffashan, Chenhui Zeng, Claudio Chuaqui, Xiaoping Hronowski, Alex Buko, Xin Zhang, and Serene Josiah. "Quality Assessment and Analysis of Biogen Idec Compound Library." Journal of Biomolecular Screening 11, no. 7 (September 14, 2006): 828–35. http://dx.doi.org/10.1177/1087057106290993.
Повний текст джерелаMbuyazi, Thandi B., and Peter A. Ajibade. "Bis(4-methylpiperidine-1-carbodithioato)-lead(II) and Bis(4-benzylpiperidine-1-carbodithioato)-lead(II) as Precursors for Lead Sulphide Nano Photocatalysts for the Degradation of Rhodamine B." Molecules 26, no. 23 (November 29, 2021): 7251. http://dx.doi.org/10.3390/molecules26237251.
Повний текст джерелаAkbari Afkhami, Farhad, Ghodrat Mahmoudi, Fengrui Qu, Arunava Gupta, Muhammet Köse, Ennio Zangrando, Fedor I. Zubkov, Ibon Alkorta, and Damir A. Safin. "Supramolecular lead(ii) architectures engineered by tetrel bonds." CrystEngComm 22, no. 13 (2020): 2389–96. http://dx.doi.org/10.1039/d0ce00102c.
Повний текст джерелаBhattacharya, Sagarika, and Sasankasekhar Mohanta. "Heterometallic copper(II)–lead(II), nickel(II)–lead(II) and copper(II)–indium(III) compounds derived from an acyclic double-compartment Schiff base ligand." Inorganica Chimica Acta 432 (June 2015): 169–75. http://dx.doi.org/10.1016/j.ica.2015.03.041.
Повний текст джерелаSingh, R. V., S. C. Joshi, Shalini Kulshrestha, Pooja Nagpal, and Anil Bansal. "Antiandrogen and Antimicrobial Aspects of Coordination Compounds of Palladium(II), Platinum(II) and Lead(II)." Metal-Based Drugs 8, no. 3 (January 1, 2001): 149–58. http://dx.doi.org/10.1155/mbd.2001.149.
Повний текст джерелаLeung, Wing-Por, Ka-Po Chan, Kwok-Wai Kan, and Thomas C. W. Mak. "Synthesis of Heteroleptic Tin(II) and Lead(II) Compounds from Pyrazyl-Linked Bisphosphoranoimine." Organometallics 27, no. 12 (June 2008): 2767–73. http://dx.doi.org/10.1021/om800104x.
Повний текст джерелаДисертації з теми "Lead (II) compounds"
Johnston, Simon Richard. "Characterisation of basic lead(II) and tin(II) compounds from aqueous systems." Thesis, Brunel University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294510.
Повний текст джерелаCaiazza, Daniela. "Crown ethers as potential lead (II) specific probes : a thesis submitted for the degree of Doctor of Philosophy /." Title page, contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phc1328.pdf.
Повний текст джерелаAbdelhamid, Dalia. "Natural Products as Lead Compounds for Drug Development. Part I: Synthesis and Biological Activity of a Structurally Diverse Library of Curcumin Analogues. Part II: Synthesis of Novel Sterol Natural Products and Related Analogues as Antileishmanial Ag." The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1299685922.
Повний текст джерелаDiantouba, Bertin Aimé. "Effets structuraux des acyl-4-pyrazolones-5 dans l'extraction liquide-liquide des cations metalliques divalents." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13093.
Повний текст джерелаCohanoschi, Mihaela. "Part I: Evaluation of Russian Synthetic Compounds as a Potential Source of New Drug Leads Agains Breast and Colon Cancer Part II: Isolation of Beta-Amyrin Formate From Eucalyptus Viminalis Labill and Investigation of its Colon Cancer Activity." Master's thesis, University of Central Florida, 2004. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/4144.
Повний текст джерелаM.S.
Department of Chemistry
Arts and Sciences
Industrial Chemistry
Caiazza, Daniela. "Crown ethers as potential lead (II) specific probes : a thesis submitted for the degree of Doctor of Philosophy / by Daniela Caiazza." Thesis, 1999. http://hdl.handle.net/2440/19405.
Повний текст джерелаBibliography: leaves 173-188.
xii, 188 leaves : ill. (chiefly col.) ; 30 cm.
Describes a comprehensive study of a select but informative set of crown ether ligands that may potentially be used in the development of a fluorescent lead (II) specific probe.
Thesis (Ph.D.)--University of Adelaide, Dept. of Chemistry, 1999
"Part I, total synthesis of (±)-pallambins C and D: and, Part II, gold-catalyzed tandem cyclization towards substituted bicyclo[3.2.1]octenone derivatives : lead to total synthesis of dhilirolides A-D." 2013. http://library.cuhk.edu.hk/record=b5549785.
Повний текст джерела本文第一章首先概述pallavicinin 系的天然源,結構特點以及生物學效用。此外,重點介紹pallambins C 和D 的分,結構鑒定以及反合成分析。
第二章討消旋體pallambins C 和D 的全合成細節。該合成以消旋Wieland-Miescher ketone (WMK)為起始原,經38 步線性步驟得到最終產物。該合成線突出以下個重要的化學轉化:a) 一個由Grob 碎及分子內aldol成環反應組成的多米式程,構建目標分子內關鍵的二環[3.2.1]辛烷酮單元;b) 一個由脲/鈀體系催化的烷氧羰基化增環反應,構建稠環型四氫呋喃/γ 內酯雙環框架。
第三章總結本文的相關研究工作。
第四章給出相關工作的詳細實驗據。
Naturally occurring pallambins A-D isolated from the Chinese liverwort Pallavicinia ambigua are classified as modified labdane-type diterpenoids, many of which exhibit interesting biological activities. From a structural perspective, pallambins C and D are consisting of trienes and an unprecedented ladder-shaped [6-5-5-5] tetracyclic skeleton bearing seven contiguous stereogenic centers. Furthermore, the bridge of the bicyclo[3.2.1]octane segment is densely substituted with two methyl groups on the bridge-heads and a vinyl group on the carbon bridge. The skeletal novelty and potential bioactivities of pallambins C and D inspired us to explore their total synthesis. In this thesis, the first total synthesis of (±)-pallambins C and D is described.
In Chapter 1, a general introduction to the natural occurrence, structural features and biological potency of pallavicinin family is presented briefly. In addition, the background of pallambins C and D including isolation, structural elucidation and retrosynthetic analysis is emphasized.
In Chapter 2, detailed synthesis of (±)-pallambins C and D involving a linear 38 steps starting from the known (±)-Wieland-Miescher ketone is discussed. The synthetic approach features the following two key conversions: a) a domino process including Grob fragmentation and intramolecular aldol cyclization to build up the bicyclo[3.2.1]octanone embedded in the target molecules; b) a thiourea/palladium-catalyzed alkoxycarbonylative annulation to assemble the fused tetrahydrofuran/γ-lactone bicyclic framework.
Chaper 3 provides a conclusion of this research work.
Chapter 4 is concerned with the experimental details.
[With images.]
Detailed summary in vernacular field only.
Detailed summary in vernacular field only.
Detailed summary in vernacular field only.
Detailed summary in vernacular field only.
Detailed summary in vernacular field only.
Xu, Xuesong.
Thesis (Ph.D.)--Chinese University of Hong Kong, 2013.
Includes bibliographical references.
Abstracts also in Chinese.
ACKNOWLEDGEMENTS --- p.I
CONTENTS --- p.II
ABBREVIATIONS --- p.V
PART I:
ABSTRACT --- p.1
Chapter CHAPTER 1. --- INTRODUCTION
Chapter 1.1 --- General background --- p.4
Chapter 1.1.1 --- General introduction to liverworts --- p.4
Chapter 1.1.2 --- General introduction to terpenoids in liverworts --- p.5
Chapter 1.2 --- Introduction to pallavicinin family --- p.9
Chapter 1.2.1 --- Isolation and structural elucidation of pallavicinin compounds --- p.9
Chapter 1.2.2 --- Synthetic advances on pallavicinin family --- p.13
Chapter 1.3 --- Introduction to the present research --- p.16
Chapter 1.3.1 --- Structural elucidation and features of pallambins C and D --- p.16
Chapter 1.3.2 --- Biogenetic hypothesis and retrosynthetic analysis of pallambins C and D --- p..20
Chapter 1.4 --- Aim of the present work --- p.22
Chapter CHAPTER 2. --- RESULTS AND DISCUSSION --- p.24
Chapter 2.1 --- Previous synthetic effort on pallambin D (2) --- p.24
Chapter 2.2 --- Successful synthetic approach to 1 and 2 --- p.25
Chapter 2.2.1 --- Synthesis of compound 24 --- p.25
Chapter 2.2.2 --- Synthesis of compound 14 --- p.30
Chapter 2.2.3 --- Synthesis of compound 13 --- p.37
Chapter 2.2.4 --- Synthesis of compound 12 --- p.43
Chapter 2.2.5 --- Synthesis of 1 and 2 --- p.53
Chapter CHAPTER 3. --- CONCLUSION --- p.60
Chapter CHAPTER 4. --- EXPERIMENTAL SECTION --- p.62
REFERENCES --- p.104
PART II:
ABSTRACT --- p.110
Chapter CHAPTER 1. --- INTRODUCTION --- p.113
Chapter 1.1 --- Introduction to bicyclo[3.2.1]octane skeleton --- p.113
Chapter 1.1.1 --- Structural features of bicyclo[3.2.1]octane --- p.113
Chapter 1.1.2 --- Bicyclo[3.2.1]octane-containing bioactive natural products --- p.114
Chapter 1.1.3 --- Methodologies for synthesis of bicyclo[3.2.1]octane derivatives --- p.116
Chapter 1.1.4 --- Gold-catalyzed construction of bicyclo[3.2.1]octane unit --- p.117
Chapter 1.2 --- Background of the present research --- p.119
Chapter 1.2.1 --- Introduction to dhilirolides A-D --- p.119
Chapter 1.2.2 --- Retrosynthetic analysis of dhilirolide A (1) --- p.121
Chapter 1.3 --- Aim of the present work --- p.122
Chapter CHAPTER 2. --- RESULTS AND DISCUSSION --- p.124
Chapter 2.1 --- Synthesis of the key acetal allene precursor 6 --- p.124
Chapter 2.1.1 --- Preparation of the starting dimethoxyl ketone 7 --- p.124
Chapter 2.1.2 --- Preparation of alkynyl furan 11 --- p.126
Chapter 2.1.3 --- Preparation of acetal allene 6 --- p.128
Chapter 2.2 --- Synthesis of bicyclo[3.2.1]octenone derivative 5 --- p.134
Chapter 2.3 --- Synthesis of mono-tosylate 26 --- p.138
Chapter CHAPTER 3. --- CONCLUSION --- p.141
Chapter CHAPTER 4. --- EXPERIMENTAL SECTION --- p.143
REFERENCES --- p.162
APPENDIX --- p.167
劉俊呈. "Finding The Lead Compounds to Suppress Protein Tyrosine Phosphatase 1B for treating Type II Diabetes by Virtual High Throughput Screening and Pharmacophore Scoring Method." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/36958358785507005380.
Повний текст джерела國立清華大學
分子醫學研究所
93
The research on the knock-out studies in mice manifests that the insulin resistance in those mice lacking for PTP1B protein would evidently increases and possesses the certain resistivity against obesity. Consequently, PTP1B is considered as the target for medicine designed to treat for Type II diabetes. With the progress in computational science, it is gradually becoming a trend to utilize the virtual screening method to accelerate the R&D in medication and effectively shorten the time and expense of R & D. In fact, there are not a few successful examples applied in foreign pharmacists. This experiment is in regard to adopting direct and indirect drug methods to screen the available inhibitor for PTP1B. First, it’s to find out the reasonable parameter computed through “DOCK” software of direct drug method towards the PTP1B receptor, the model based on the aforementioned parameter, which correlation can reach 0.79 in the activity ranks of inhibitor, then to proceed the virtual screening in “Maybridge” chemistry database. On the other hand, to establish the pharmacoophore which the so-called “Catalyst” indirect drug method software applied in screening PTP1B inhibitor, then reaching 0.976 correlation and 0.868 rms following this step, to make the activity predict on the compound screened by the DOCK software. In addition to this, assorting with two scoring function in terms of XScore and PScore, and the screening method of hydrogen bond, at last select 165 most potential lead compounds of PTP1B.
DiDonato, Dana A. "Part I. design and synthesis of prototypes as leads on a compound library aimed at plasmepsin ii inhibition. Part II. synthesis and evaluation of modified nucleotides for dna aptamer selection." 2006. http://www.lib.ncsu.edu/theses/available/etd-08042006-151854/unrestricted/etd.pdf.
Повний текст джерелаWang, Ying-Lien, and 王櫻璉. "(I) The Design and Synthesis of Benzimidazole and Dihydroquinazolines Derivatives Based on Lead Compound (II) Ruthenium-Catalysed C-H activation to the Synthesis of [4,5]imidazo[2,1-a]isoindole Derivatives." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/71056344608467361199.
Повний текст джерелаКниги з теми "Lead (II) compounds"
Dub, Michael. Organometallic Compounds Literature Survey 1937-1958: Volume II Organic Compounds of Germanium, Tin and Lead. Springer London, Limited, 2013.
Знайти повний текст джерелаЧастини книг з теми "Lead (II) compounds"
Huber, F., and K. Grätz. "From Lead(II) Compounds with Organoalkali Reagents." In Inorganic Reactions and Methods, 214. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145258.ch67.
Повний текст джерелаCrisp, G. T. "Using Magnesium and Lead(II) Bromide." In Compounds of Group 14 (Ge, Sn, Pb), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00467.
Повний текст джерелаGuiry, P. J., and P. J. McCormack. "Reaction of Halotriorganoplumbanes with Lead(II) Thiolates." In Compounds of Group 14 (Ge, Sn, Pb), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00710.
Повний текст джерела"20. Introduction of Fluorine with Lead(II) Fluoride and Organolead Fluorides." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Stuttgart: Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111184.
Повний текст джерелаEagle, P. A. C. "Tetrabenzylplumbanes from Lead(II) Chloride and Benzylmagnesium Halides." In Compounds of Group 14 (Ge, Sn, Pb), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00804.
Повний текст джерелаEagle, P. A. C. "From Lead(II) Chloride, Grignard Reagents, and Allyl Halides." In Compounds of Group 14 (Ge, Sn, Pb), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00811.
Повний текст джерелаEmsley, John. "Lead murders." In The Elements of Murder. Oxford University Press, 2005. http://dx.doi.org/10.1093/oso/9780192805997.003.0021.
Повний текст джерелаEagle, P. A. C. "Benzylplumbanes from Lead(II) Chloride, Arylmagnesium Bromides, and Benzyl Halides." In Compounds of Group 14 (Ge, Sn, Pb), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00805.
Повний текст джерелаEagle, P. A. C. "Alkyl(trivinyl)plumbanes from Lead(II) Chloride by Reactions with Vinylmagnesium Halides and Haloalkanes." In Compounds of Group 14 (Ge, Sn, Pb), 1. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-005-00796.
Повний текст джерелаKoli, Preeti, and Rajesh K. Singh. "Progress in Nitrogen and Sulphur-based Heterocyclic Compounds for their Anticancer Activity." In Key Heterocyclic Cores for Smart Anticancer Drug–Design Part II, 79–104. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815040043122020006.
Повний текст джерелаТези доповідей конференцій з теми "Lead (II) compounds"
Ouvaroff, A. A., I. A. Butko, and N. A. Litova. "Physico-chemical properties and ecological aspect of crystalline iron (III) orthovanadate, iron (III), copper (II) and lead (II) metavanadate." In III All-Russian Scientific Conference with International Participation "Science, technology, society: Environmental engineering for sustainable development of territories". Krasnoyarsk Science and Technology City Hall, 2022. http://dx.doi.org/10.47813/nto.3.2022.6.125-136.
Повний текст джерелаJain, Sukriti, and Pritpal Singh. "Electrodeposition and Characterization of Very Thin Film II-VI Compounds for Novel Superlattice Solar Cells." In ASME 2010 4th International Conference on Energy Sustainability. ASMEDC, 2010. http://dx.doi.org/10.1115/es2010-90239.
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Повний текст джерелаBurger, Victor, Andy Yates, Thomas Mosbach, and Barani Gunasekaran. "Fuel Influence on Targeted Gas Turbine Combustion Properties: Part II — Detailed Results." In ASME Turbo Expo 2014: Turbine Technical Conference and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/gt2014-25105.
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