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Relevant bibliographies by topics / Derivatives 5

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Academic literature on the topic 'Derivatives 5'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Derivatives 5"

1

Drašar, Pavel, and Jiří Beránek. "2',3'-O-Carbonyl derivatives of 6-azauridine in the synthesis of its 5-substituted and 5'-deoxy derivatives." Collection of Czechoslovak Chemical Communications 52, no. 8 (1987): 2070–82. http://dx.doi.org/10.1135/cccc19872070.

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Preparation of 2',3'-O-carbonyl derivatives of 5'-deoxy-6-azauridine and 6-azauridine using 1,1'-carbonyldiimidazole has been elaborated. 5'-Chloro and 5'-bromo derivatives were prepared by treatment of the 5'-O-mesyl derivative with quaternary ammonium halides, 5'-chloro derivatives also by direct halogenation with thionyl chloride in hexamethylphosphortriamide or with tetrachloromethane, triphenyl phosphine, and dimethylformamide. Derivatives of 5'-bromo-6-azauridine were reduced with tributyltin hydride to 5'-deoxy-6-azauridine compounds. 6-Azauridine 2',3'-carbonate (IVa) and its 5'-deriva

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2

Liu, Xin-Hua, Bao-An Song, Pinaki S. Bhadury, et al. "Novel 5-(3-(Substituted)-4,5-dihydroisoxazol-5-yl)-2-methoxyphenyl Derivatives: Synthesis and Anticancer Activity." Australian Journal of Chemistry 61, no. 11 (2008): 864. http://dx.doi.org/10.1071/ch07395.

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Thirty novel 5-(3-(substituted phenyl)-4,5-dihydroisoxazol-5-yl)-2-methoxyphenyl derivatives were synthesized and evaluated for their antitumour activity. The bioassays showed that the 2-fluorobenzoyl derivative 6ai, the 4-trifluoromethylbenzoyl derivative 6ah, and the 3-trifluoromethyl isoxazole derivatives (6ch and 6ci) were highly effective against PC-3 cells. The IC50 values of 6ah and 6ai against PC-3 cells were 1.5 and 1.8 μg mL–1, respectively.

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Krečmerová, Marcela, Hubert Hřebabecký, and Antonín Holý. "Synthesis of 5-Phenylcytosine Nucleoside Derivatives." Collection of Czechoslovak Chemical Communications 61, no. 4 (1996): 645–55. http://dx.doi.org/10.1135/cccc19960645.

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Reaction of silylated 5-phenylcytosine with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribose, catalyzed with tin tetrachloride, and subsequent methanolysis afforded 5-phenylcytidine (2). This compound reacted with thionyl chloride in acetonitrile to give cyclic sulfite 3 which on heating in dimethylformamide was converted into 2,2'-anhydro-1-(β-D-arabinofuranosyl)-5-phenylcytosine (4). Analogous reaction of compound 2 with thionyl chloride at reflux gave 5'-chloro-5'-deoxy-2',3'-cyclic sulfite 5. Its heating in dimethylformamide afforded 5'-chloro-2,2'-anhydro derivative 6, mild alkaline hydrolysis led

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4

Persson, T., A. B. Hörnfeldt, S. Gronowitz та N. G. Johansson. "Synthesis of Mimics to 5-(2″-thienyl)-2′,3′-β-Dideoxyuridine Triphosphate". Antiviral Chemistry and Chemotherapy 7, № 2 (1996): 101–7. http://dx.doi.org/10.1177/095632029600700207.

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A series of 5′-amido derivatives of 5-(2″-thienyl)-2′,3′,5′-β-trideoxyuridine were prepared. The compounds were tested for their inhibition of cellular DNA polymerase α and α HIV-RT. The succinic fumaric and maleic acid derivatives of 5-(2″-thienyl)-2′,3′,5′-β-trideoxyuridine were investigated. None of the compounds inhibited HIV-RT. The fumaric acid derivative inhibited DNA pol α with IC50 33 μg ml−1. The succinic acid derivative was about half as active with IC50 76 μg ml−1. The 5′-N-acyl derivatives also were structurally compared to the monomethyl ester of the triphosphate using the Sybyl

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5

Mistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Chalcone, Pyrazoline, Pyrimidine - 2 - One, Pyrimidine - 2 - Thione,para-Acetanilide Sulphonyl and Benzoyl Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 30–41. http://dx.doi.org/10.1155/2005/953107.

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1, 2 - Dichloro benzene on chlorosulphonation by chlorosulphonic acid gives 1, 2 - [dichloro] - benzene sulphonyl chloride which on condensation withp–amino acetophenone gives 1-[acetyl] - 1’ , 2’ - [dichloro] - dibenz sulphonamide derivative. This derivative undergo condensation with 2,4- dichloro benzaldehyde gives 1- [3” - (sub. phenyl) - 2” - propene - 1” - one] - 1’ , 2’ - [dichloro] - dibenz sulphonamide derivative which on reaction with 99% hydrazine hydrate and glacial acetic acid gives 1-[acetyl]-3- [1’ , 2’ - (dichloro) - dibenz sulphonamide] -5 - [2” , 4” - dichloro phenyl] - 2 - py

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6

Journal, Baghdad Science. "Synthesis and Characterization of New Heterocyclic Compounds from 2, 5- dimercapto -1, 3, 4-Thiadiazole and Their Resins." Baghdad Science Journal 13, no. 2 (2016): 275–88. http://dx.doi.org/10.21123/bsj.13.2.275-288.

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In this research, a new 1, 3, 4-Thiadiazole derivatives have been synthesized by many heterocyclic reactions. Starting from (2, 5 – dimercapto -1, 3, 4-Thiadiazole) a variety of derivatives have been synthesis. Compound (1) was synthesized by the reaction of hydrazine hydrate with carbon disulphide in absolute ethanol. The compound (1) was reacted with 1, 2-dibromoethane in presence of alkali ethanol to give the compound (2). The compound (3) was formed from the reaction of compound (2) with hydrazine hydrate. Schiff base (4) was obtained by reacting of compound (3) with the compound (p-hydrox

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7

Engesser, Tobias, and Reinhard Brückner. "Stereoselective Aldol Additions of Glycolic Acid and Its Derivatives." Synthesis 51, no. 08 (2019): 1715–45. http://dx.doi.org/10.1055/s-0037-1611721.

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This review gives a comprehensive overview of aldol additions of glycolic acid derivatives to achiral aldehydes and acetals affording α,β-dihydroxycarboxylic acids or derivatives thereof. The focus is on simple diastereoselectivity. A selection of related aldol additions is also presented: aldol additions of glycolic acid derivatives to ketones with two different substituents and aldol additions of α-substituted glycolic acid derivatives.1 Introduction1.1 Organization of this Review1.2 Outside the Scope of this Review: Aldol Additions Giving α,β-Dihydroxyaldehydes and α,β-Dihydroxyketones Dias

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Holý, Antonín, Joachim König, Jiří Veselý, Dieter Cech, Ivan Votruba, and Erik De Clercq. "5'-O-Alkyl-5-fluorouridines: Synthesis and biological activity." Collection of Czechoslovak Chemical Communications 52, no. 6 (1987): 1589–608. http://dx.doi.org/10.1135/cccc19871589.

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Methyl 2,3-O-isopropylidene-D-ribofuranoside (IV) was alkylated with alkyl halides in the presence of sodium hydride and the products were transformed by acid hydrolysis and glycosylation into methyl 5-O-alkyl-D-ribofuranosides VII. Benzoylation of VII followed by acetolysis afforded 1-O-acetyl-2,3-di-O-benzoyl-5-O-alkyl-D-ribofuranoses IX which on reaction with 2,4-bis(trimethylsilyloxy)pyrimidine in the presence of tin tetrachloride in acetonitrile and subsequent hydrolysis gave 5'-O-alkyl-2',3'-di-O-benzoyluridines XIa-XIe. Methanolysis of compounds XI furnished 5'-O-alkyluridines III. The

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9

Mistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Azlactone Derivatives and Imidazolinone Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 42–51. http://dx.doi.org/10.1155/2005/542938.

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p- Methyl benzoic acid on reaction with phosphorus pentachloride gives p - methyl benzoyl chloride derivative which on condensation with glycine gives p - methyl benzoyl glycine derivative. Now, this p - methyl benzoyl glycine derivative on condensation with various substituted aldehydes gives corresponding substituted 4 - [aryl methylidine] - 2 - [p - methyl phenyl] - oxazole - 5 - one derivatives [1(a-j)]. Further, these derivatives [1(a-j)] on condensation with 4 , 4’ - diamino diphenyl sulphone gives corresponding substituted imidazolinone - dibenzsulphone derivatives [2(a-j)], on condensa

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Dutta, Saikat, Linglin Wu, and Mark Mascal. "Production of 5-(chloromethyl)furan-2-carbonyl chloride and furan-2,5-dicarbonyl chloride from biomass-derived 5-(chloromethyl)furfural (CMF)." Green Chemistry 17, no. 7 (2015): 3737–39. http://dx.doi.org/10.1039/c5gc00936g.

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Biomass-derived CMF is oxidized to the acid chloride CMFCC in a single step using inexpensive t-butyl hypochlorite. Likewise, DFF, also a CMF derivative, is oxidized directly to the diacid chloride FDCC. The products are platforms for a variety of chemical derivatives of carbohydrates.

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Dissertations / Theses on the topic "Derivatives 5"

1

Aw, Leonard Kah Jin. "Some chemistry of 5-diazouracil and its derivatives." Thesis, City University London, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328892.

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Gao, Xuefeng Harmata Michael. "Oxidation & 1, 5-hydride shift of sulfoximine derivatives." Diss., Columbia, Mo. : University of Missouri--Columbia, 2009. http://hdl.handle.net/10355/6646.

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Title from PDF of title page (University of Missouri--Columbia, viewed on March 10, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Thesis advisor: Dr. Michael Harmata. Includes bibliographical references.

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Chornous, V. O. "5-carbofunctionalized imidazoles and their derivatives: synthesis and biomedical investigation." Thesis, БДМУ, 2017. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/16859.

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Flynn, Bernard L. "The synthesis and palladium-catalysed coupling of 5-Trifluoromethanesulfonyluridine derivatives /." Title page, contents and abstractn only, 1992. http://web4.library.adelaide.edu.au/theses/09PH/09phf648.pdf.

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Borssum, Waalkes Marjan van. "Lipophilic derivatives of 5-fluoro-2'-deoxyuridine as liposomal anticancer agents." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 1992. http://irs.ub.rug.nl/ppn/292987617.

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Kayalar, Metin. "Synthesis Of 1,2,3,5-tetrasubstituted Pyrrole Derivatives Via 5-exo-dig Type Cyclization And Stereoselective Functionalisation Of Ferrocene Derivatives." Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/12605757/index.pdf.

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ABSTRACT SYNTHESIS OF 1,2,3,5-TETRASUBSTITUTED PYRROLE DERIVATIVES VIA 5-EXO-DIG TYPE CYCLIZATION AND STEREOSELECTIVE FUNCTIONALISATION OF FERROCENE DERIVATIVES Metin Kayalar M.S., Department of Chemistry Supervisor: Prof. Dr. Ayhan S. Demir January 2005, 102 pages A convenient and new method for the synthesis of 1,2,3,5-tetrasubstituted pyrrole derivatives starting from 1,3,-dicarbonyl compounds through acid catalyzed cyclization reaction is described. Alkylation of 1,3-dicarbonyl compound with propargyl bromide followed by one step cyclization with the introduction of primary amines in

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7

Erdtman, Edvin. "5-Aminolevulinic acid and derivatives thereof : properties, lipid permeability and enzymatic reactions." Doctoral thesis, Örebro universitet, Akademin för naturvetenskap och teknik, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-9951.

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5-aminolevulinic acid (5-ALA) and derivatives thereof are widely usedprodrugs in treatment of pre-malignant skin diseases of the cancer treatmentmethod photodynamic therapy (PDT). The target molecule in 5-ALAPDTis protoporphyrin IX (PpIX), which is synthesized endogenously from5-ALA via the heme pathway in the cell. This thesis is focused on 5-ALA,which is studied in different perspectives and with a variety of computationalmethods. The structural and energetic properties of 5-ALA, itsmethyl-, ethyl- and hexyl esters, four different 5-ALA enols, and hydrated5-ALA have been investigated using Q

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8

Sullivan, Shannon M. "Synthesis of 2,4-disubstituted pyrimidine derivatives as potential 5-HT7 receptor antagonist." unrestricted, 2008. http://etd.gsu.edu/theses/available/etd-05052008-153400/.

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Thesis (M.S.)--Georgia State University, 2008.<br>Title from file title page. Lucjan Strekowski, committee chair; A.L. Baumstark, Gabor Patonay, Doyle Barrow , committee members. Electronic text (68 p. : ill.) : digital, PDF file. Description based on contents viewed June 23, 2008. Includes bibliographical references (p. 42-430.

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9

Ireland, Alan C. "Metabolism and mode of action of 5-aminosalicylic acid and its derivatives." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236211.

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Jorge, Salomão Dória. "Síntese e avaliação da atividade antibacteriana de derivados 5-metilsulfonil-2-tiofilidênicos e de derivados 5(6)-benzofuroxânicos frente a cepas padrão e multi-resistente de Staphylococcus aureus." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/9/9135/tde-20062007-143516/.

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A emergência de resistência microbiana é um desafio para microbiologistas, médicos, órgãos de saúde pública e para a indústria farmacêutica. Passado três décadas, patógenos gram-positivos, principalmente Staphylococcus aureus, têm desenvolvido cada vez mais resistência a vários antibióticos devido ao uso extensivo nos hospitais e na comunidade. Este desenvolvimento aconteceu em um período em que poucas novas classes de antibióticos tenham sido identificadas, ressaltando a necessidade urgente de novos agentes antimicrobianos. A modificação molecular tem se mostrado como estratégia bastante prom

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Books on the topic "Derivatives 5"

1

McKinnell, Denise. Phototransformation of 5-[inferior t]-butyl uracil derivatives. University of Birmingham, 1997.

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2

United States. Congress. House. Committee on Ways and Means. Subcommittee on Select Revenue Measures. Derivatives: Hearing before the Subcommittee on Select Revenue Measures of the Committee on Ways and Means, U.S. House of Representatives, One Hundred Tenth Congress, second session, March 5, 2008. U.S. G.P.O., 2011.

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3

Das, Satyajit, ed. Risk Management and Financial Derivatives. Palgrave Macmillan UK, 1997. http://dx.doi.org/10.1007/978-1-349-14605-5.

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Dewan, Mohamed Essa. Modification of polyethylene by radiation induced grafting with 5-vinylsalicylic acid derivatives. University of Salford, 1993.

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5

Slater, Martin John. The synthesis and properties of some 5-substituted derivatives of 2'- deoxyuridine. University of Birmingham, 1985.

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6

Bouchard, Bruno, and Jean-François Chassagneux. Fundamentals and Advanced Techniques in Derivatives Hedging. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-38990-5.

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Oliveira, Carlos. Options and Derivatives Programming in C++23. Apress, 2023. http://dx.doi.org/10.1007/978-1-4842-9827-5.

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Jørgensen, Poul, and Jack Simons, eds. Geometrical Derivatives of Energy Surfaces and Molecular Properties. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4584-5.

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Raman, Maya, Abhilash Sasidharan, S. Sabu, and Dhanya Pulikkottil Rajan, eds. Fish Structural Proteins and its Derivatives: Functionality and Applications. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-2562-5.

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International Symposium on Superalloys 718, 625, 706 and Various Derivatives (6th 2005). Superalloys 718, 625, 706 and various derivatives: Proceedings of the Sixth International Symposium on Superalloys 718, 625, 706 and Various Derivatives : held October 2-5, 2005. TMS, 2005.

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Book chapters on the topic "Derivatives 5"

1

Raol, Jitendra R., and Jatinder Singh. "Aerodynamic Derivatives." In Flight Mechanics Modeling and Analysis, 2nd ed. CRC Press, 2023. http://dx.doi.org/10.1201/9781003293514-5.

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Dufournier, Philippe. "Case Study." In Derivatives Unlocked. Chapman and Hall/CRC, 2024. https://doi.org/10.1201/9781003485841-5.

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Hastings, Kevin J. "Valuation of Derivatives." In Introduction to Financial Mathematics, 2nd ed. Chapman and Hall/CRC, 2024. http://dx.doi.org/10.1201/9781003287278-5.

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Yang, Xiao-Jun. "Fractional Derivatives of Variable Order with Respect to Another Function and Applications." In General Fractional Derivatives. Chapman and Hall/CRC, 2019. http://dx.doi.org/10.1201/9780429284083-5.

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Koeber, Karl, Helga Köttelwesch, Dietrich Schneider, Helga Demmer, and Edith Schleitzer-Rust. "Complexes with Derivatives of Hydroxylamine." In Mn Manganese D 5. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-662-08175-4_6.

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Koeber, Karl, Helga Köttelwesch, Dietrich Schneider, Helga Demmer, and Edith Schleitzer-Rust. "Complexes with Hydrazinecarboxylic Acid and Derivatives." In Mn Manganese D 5. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-662-08175-4_3.

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Kagel, John R., James L. Kofron, and Daniel H. Rich. "Synthesis of 5-fluoroproline derivatives." In Peptides. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_331.

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Cowell, Frances. "Appendix 5: Options." In Practical Quantitative Investment Management with Derivatives. Palgrave Macmillan UK, 2002. http://dx.doi.org/10.1057/9780230501874_26.

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Arias-Barrera, Ligia Catherine. "The Problem of Environmental Risks and Uncertainties in ESG Derivatives." In The Law of ESG Derivatives. Routledge, 2024. http://dx.doi.org/10.4324/9781003365242-5.

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Argyros, Ioannis K. "A Novel Scheme Free from Derivatives." In The Theory and Applications of Iteration Methods, 2nd ed. CRC Press, 2021. http://dx.doi.org/10.1201/9781003128915-5.

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Conference papers on the topic "Derivatives 5"

1

Mih�ly, Norbert B., Miruna Prodan, Vasile M. Cristea, and Anton A. Kiss. "Sustainable Downstream Process Design for HMF Conversion to Value-Added Chemicals." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.185398.

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Biomass conversion to chemical derivatives and essential intermediates is regarded as a long-term strategy for the chemical sector. Among the numerous valuable chemicals obtained from biomass, 5-hydroxymethylfurfural (HMF) is considered an industrially relevant compound due to its capacity to be converted into a variety of value-added chemicals. Compared to conventional catalytic synthesis, bio-catalysis has emerged as a potential greener substitute for HMF conversion to value-added compounds. HMF conversion through bio-catalysis, although more sustainable, seldom leads to the production of a

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Ivanov, Maxim A., Inna L. Karpenko, Eduard R. Shmalenyuk та Lyudmila A. Alexandrova. "New α-thymidine 5'-phosphonate derivatives". У XVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112342.

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Krečmerová, Marcela, and Antonín Holý. "Synthesis of C-5 substituted HPMPC (cidofovir) derivatives." In XIIIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507287.

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Welchinskaya, Elena. "CHEMISTRY AND ANTITUMOUR ACTIVITY OF 5-BROMOURACILE’S DERIVATIVES." In CBU International Conference on Integration and Innovation in Science and Education. Central Bohemia University, 2013. http://dx.doi.org/10.12955/cbup.2013.45.

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Shmalenyuk, Eduard R., Maxim A. Ivanov, Inna L. Karpenko, and Lyudmila A. Alexandrova. "Synthesis and some biological properties of 5-alkoxymethyl derivatives of 2'-deoxyuridine 5'-phosphonates." In XVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112457.

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Arbin, M., N. Ahmat, and M. Taha. "Synthesis and thymidine phosphorylase inhibition studies of 5-chlorobenzothiazole derivatives." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608216.

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Ariza-Rúa, Danilo, Liliana Carranza-López, Edisson Chavarro-Mesa, Julio Hurtado Márquez, and Humberto Marbello-Peña. "2D-QSAR Study of Thiazole derivatives as 5-Lipoxygenase inhibitors." In 22nd LACCEI International Multi-Conference for Engineering, Education and Technology (LACCEI 2024): “Sustainable Engineering for a Diverse, Equitable, and Inclusive Future at the Service of Education, Research, and Industry for a Society 5.0.”. Latin American and Caribbean Consortium of Engineering Institutions, 2024. http://dx.doi.org/10.18687/laccei2024.1.1.1785.

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Smirnova, Olga A., and Ludmila A. Alexandrova. "Synthesis of 5-(N-hydroxy)- and 5-(N-alkoxy)carboxamido derivatives of uridine and uracile." In XIVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2008. http://dx.doi.org/10.1135/css200810302.

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Nedeljković, Nikola V., Vladimir D. Dobričić, Marina Ž. Mijajlović, et al. "„IN SILICO“ PREDICTION OF PHARMACOKINETIC PROPERTIES AND DRUGLIKENESS OF NOVEL THIOUREA DERIVATIVES OF NAPROXEN." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.371n.

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Masking the carboxyl group of naproxen with other functional groups may be a promising strategy to decrease its gastrointestinal toxicity. Thiourea moiety has been described as an important pharmacophore in a variety of pharmacologically active compounds, including anti-inflammatory, antiviral, anticancer, hypoglycemic and antimicrobial agents. Our research group has previously designed twenty novel thiourea derivatives of naproxen, containing amino acids (glycine, L-alanine, β-alanine, L-valine and L-phenylalanine – compounds 1,2,3,4 and 5, respectively), their methyl (6–10) and ethyl esters

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Balandis, Benas, Kazimieras Anusevičius, Vytautas Mickevičius, Maryna Stasevych, and Volodymyr Novikov. "Synthesis and antibacterial activity of novel 3-substituted 1-(2-methyl-5-nitrophenyl)-5-oxopyrrolidine derivatives." In Chemical technology and engineering. Lviv Polytechnic National University, 2019. http://dx.doi.org/10.23939/cte2019.01.247.

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Reports on the topic "Derivatives 5"

1

Axenood, Theodore, Jianguang Sun, and Kakal K. Dad. Synthesis and Characterization of 5-Substituted-1,3-Diazacyclohecane Derivatives. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada360626.

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Thomashow, Linda, Leonid Chernin, Ilan Chet, David M. Weller, and Dmitri Mavrodi. Genetically Engineered Microbial Agents for Biocontrol of Plant Fungal Diseases. United States Department of Agriculture, 2005. http://dx.doi.org/10.32747/2005.7696521.bard.

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The objectives of the project were: a) to construct the site-specific integrative expression cassettes carrying: (i) the chiA gene for a 58-kDa endochitinase, (ii) the pyrrolnitrin biosynthesis operon, and (iii) the acdS gene encoding ACC deaminase; b) to employ these constructs to engineer stable recombinant strains with an expanded repertoire of beneficial activities; c) to evaluate the rhizosphere competence and antifungal activity of the WT and modified strains against pathogenic fungi under laboratory and greenhouse conditions; and d) to monitor the persistence and impact of the introduce

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Carson, J. M., P. B. Holman, R. B. K. Shives, K. L. Ford, C T Harper, and W. Slimmon. Magnetic first vertical derivative map, Mukasew Lake, Saskatchewan, NTS 64M/5. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2001. http://dx.doi.org/10.4095/212455.

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Schwartz, J. L., J. M. Cowan, E. Moan, B. A. Sedita, J. Stephens, and A. T. M. Vaughan. Metaphase chromosome and nucleoid differences between CHO-K1 and its radiosensitive derivative xrs-5. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10149006.

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Dumont, R., and J. Potvin. First vertical derivative of the total magnetic field, aeromagnetic survey Baffin Island 2005, 36 A/5, Nunavut. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2006. http://dx.doi.org/10.4095/222317.

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Dumont, R., and J. Potvin. First vertical derivative of the total magnetic field, aeromagnetic survey Baffin Island 2005, 36 B/5, Nunavut. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2006. http://dx.doi.org/10.4095/222325.

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Coyle, M., and F. Kiss. First vertical derivative of the magnetic field, Partridge Breast Lake aeromagnetic survey, Wood Lake, NTS 64 H/5, Manitoba. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2008. http://dx.doi.org/10.4095/226033.

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Kiss, F., and M. Coyle. First vertical derivative of the magnetic field, aeromagnetic survey of the Nisling River area, NTS 115 J/5, 6, Yukon. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2011. http://dx.doi.org/10.4095/288949.

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Kiss, F., and M. Coyle. First vetical derivative of the magnetic field, Hottah Lake aeromagnetic survey, parts of NTS 86 C/5, 12, 86 D/5, 6, 7, 8, 9, 10, 11, 12, Northwest Territories. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2011. http://dx.doi.org/10.4095/288788.

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Dumont, R., and J. Potvin. First vertical derivative of the total magnetic field, aeromagnetic survey Baffin Island 2005, 36 A/8 and 26 D/5, Nunavut. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2006. http://dx.doi.org/10.4095/222320.

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