Relevant bibliographies by topics / Anilides

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Anilides'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Anilides"

1

Shteinberg, Leon. "INFLUENCE OF SUBSTITUTES ON THE RATE OF THE REACTION OF ORTHOSUBSTITUTED BENZOIC ACIDS WTH ANILINE, CATALYZED BY POLYBUTOXYTITANATES." Ukrainian Chemistry Journal 87, no. 3 (2021): 18–40. http://dx.doi.org/10.33609/2708-129x.87.03.2021.18-40.

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The polybutoxytitanates catalysis of aniline acylation by orthosubstituted benzoic acids leads to the production of substituted benzanilides. Catalytic rate constants of the second order reaction (the first with respect to aniline and ortho-substituted benzoic acid; boiling ortho=xylene, 145°C) correlate well according to the Hammett and Bronsted equations with straight line segments with ρ=1.93 and α=0.66, in contrast to the reaction of aniline with meta- and parasubstituted benzoic acids and substituted anilines with benzoic acid. This dependence drops out 2=nitrobenzoic and 1=naphthoic acid
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Mieriņa, Inese, Darja Kostjuņina, Dārta Zelma Skrastiņa, and Mara Jure. "Synthesis and Antiradical Activity of 2-Arylidenemalonic Acid Dianilides." Key Engineering Materials 850 (June 2020): 230–35. http://dx.doi.org/10.4028/www.scientific.net/kem.850.230.

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The most common cinnamoyl anilines are avenanthramides, which are natural antioxidants found in oats. This is a rather uncommon and not well-investigated group of antioxidants. This paper deals with 2-arylidenemalonic acid dianilides – cinnamoyl anilines which are decorated with an additional arylaminocarbonyl moiety at α-position of double bond. The DPPH scavenging activity of the title compounds is slightly lower in comparison to the corresponding cinnamoyl anilines. On the other hand, the title dianilides are more active than cinnamic acid anilides containing an additional carboxylic group
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Shteinberg, Leon. "CATALYSIS OF TRIVALENT PHOSPHORUS COMPOUNDS OF THE REACTIONS OF SUBSTITUTED BENZOIC ACIDS WITH ANILINE." Ukrainian Chemistry Journal 88, no. 6 (2022): 102–20. http://dx.doi.org/10.33609/2708-129x.88.06.2022.102-120.

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The catalytic preparation of substituted benzanilides by the reaction of substituted benzoic acids with aniline is an important model process that has been intensively deve­lo­ped recently, in the field of the «green chemistry» concept, direct catalytic amidation, and its study is an urgent scientific and practical task.
 Within the framework of solving this problem, the catalysis of the acylation of aniline by substituted benzoic acids with trivalent phosphorus compounds P(III) was studied. It was established that P(III) in the amount of only 2% mol. from substituted benzoic acid effecti
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Shteinberg, Leon. "CATALYSIS BY PHOSPHORUS AND SILICON COMPOUNDS IN THE SYNTHESIS OF OXYNAPHTOIC ACID ANILIDES." Ukrainian Chemistry Journal 89, no. 1 (2023): 46–59. http://dx.doi.org/10.33609/2708-129x.89.01.2023.46-59.

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Catalysis of the acylation of aniline with 3-­hydroxy-2-naphthoic, 1-hydroxy-2-naphthoic, 2-hydroxy-1-naphthoic and 1-hydroxy-4-naphthoic acids by phosphorus P(III) and silicon Si(IV) compounds leads to the formation anilides of the corresponding hydroxy­naphthoic acids under mild conditions (ortho-xylene, 146.5–147 °C) in almost quantitative yield.
 Among P(III) phosphorus trichloride and tribromide; phosphorous, 1-hydroxyethyli­de­ne-di­phos­phonic, pyrophosphorous and me­ta­phos­phorous acids; trimethyl-, dimethyl- and diethylphosphites; phosph(III)azan proved to be active catalysts; a
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P., K. Dubey, and Vinod Kumar R. "Reactions of aniline with unsymmetrical acid anhydrides." Journal of Indian Chemical Society Vol. 78, May 2001 (2001): 265–66. https://doi.org/10.5281/zenodo.5878448.

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Department of Chemistry, College of Engineering, J. N. T. University, Kukatpally, Hyderabad-500 072, India <em>E-mail</em>: jntuc@ap.nic.in&nbsp; &nbsp;<em>Fax</em>: 91-040-3056506 <em>Manuscript received 4 October 1999, revised 30 June 2000, accepted 20 December 2000</em> Reaction of aniline with some mixed/unsymmetrical acid anhydrides to give exclusively one of the anilides is described.
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Liu, Yilin, Xiangqing Feng, and Haifeng Du. "Asymmetric synthesis of axially chiral anilides by Pd-catalyzed allylic substitutions with P/olefin ligands." Organic & Biomolecular Chemistry 13, no. 1 (2015): 125–32. http://dx.doi.org/10.1039/c4ob01087f.

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Wang, Yang, Ying Wang, Qian Zhang, and Dong Li. "Site-selective oxidative C–H sulfonylation of 8-acylaminoquinolines and anilides under metal-free conditions." Organic Chemistry Frontiers 4, no. 4 (2017): 514–18. http://dx.doi.org/10.1039/c6qo00730a.

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A highly site-selective oxidative C–H sulfonylation method for 8-acylaminoquinolines and anilides with sulfonyl chlorides has been developed, which provided C5-sulfonylated quinolines and para-sulfonylated anilides respectively.
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de Jonge, A. P. "Acid anilides: I. Preliminary communication on the chromatography of acid anilides." Recueil des Travaux Chimiques des Pays-Bas 74, no. 6 (2010): 760–62. http://dx.doi.org/10.1002/recl.19550740614.

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Gledhill, L., P. Williams та B. W. Bycroft. "Irreversible inactivation of β-lactamase I from Bacillus cereus by chlorinated 6-spiroepoxypenicillins". Biochemical Journal 276, № 3 (1991): 801–7. http://dx.doi.org/10.1042/bj2760801.

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On incubation of the chlorinated 6-spiroepoxypenicillin anilides (I) and (II) [formula: see text] with beta-lactamase 1 from Bacillus cereus, three distinct processes are observed. The inhibitors act as (a) substrates, the turnover of which respectively results in a single product, namely 6-substituted 2(H)-3,4-dihydro-1,4-thiazine, (b) a transiently inhibited enzyme complex, and finally (c) an irreversibly inactivated enzyme complex. Although differing only in their stereochemistry at one centre, the anilide (K) is a more potent irreversible inactivator of beta-lactamase I than is compound (I
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Ates, Ali, and Dennis P. Curran. "Synthesis of Enantioenriched Axially Chiral Anilides from Atropisomerically Enriched Tartarate Ortho-Anilides." Journal of the American Chemical Society 123, no. 21 (2001): 5130–31. http://dx.doi.org/10.1021/ja010467p.

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Dissertations / Theses on the topic "Anilides"

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Hughes, Adam D. "New stereoselective enolate chemistry using atropisomeric anilides." Thesis, University of Nottingham, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266925.

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Desai, Salil Dileep Kirsch Lee E. "Ortho substitution effects on the acidic and alkaline hydrolyses of formanilides." [Iowa City, Iowa] : University of Iowa, 2009. http://ir.uiowa.edu/etd/353.

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Mendiratta, Arjun. "Reductive coupling and related reactions with Mo and Ti tris- anilides." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/32483.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2005.<br>Vita.<br>Includes bibliographical references.<br>Chapter 1: The capability of Mo(N[t-BulAr)₃ to act as a powerful one, two, and three electron reductant have been previously demonstrated. In this work, we show that Mo(NIt-BulAr)₃ forms a metastable adduct with the moderate [pi] acid PhCN; coordination of PhCN activates the nitrile carbon towards reaction with a variety of one-electron reagents such as dichalcogenides, nitric oxide, hydrogen atom donors, cobaltocene, and elemental phosphorus. Evidence is presen
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Dufour, Jérémy. "Synthèses totales des arylomycines A₂ et B₂études vers la synthèse des TMC-95Nouvelle voie d’accès à des oxindoles par fonctionnalisation C-H palladocatalysée." Paris 11, 2009. http://www.theses.fr/2009PA112209.

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Les molécules macrocycliques comportant une liaison aryle-aryle endocyclique, en vertu de leurs activités biologiques diverses ont joué et jouent encore un rôle clé dans l’élaboration de nouveaux médicaments. L’essentiel de ce travail a été consacré à l’étude vers la synthèse totale de deux familles de molécules de ce type récemment isolées : le arylomycines, inhibiteurs de la peptidase signal I des bactéries, et les TMC-95, inhibiteurs du protéasome. Tout d’abord, nous avons réalisé des synthèses totales des arylomycines A2 et B2 de manière convergente et concise. La préparation du macrocycle
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Devault, Damien Lim Puy Pinelli Eric. "Approche spatio-temporelle de la contamination par les herbicides de pré-levée du biotope de la Garonne Moyenne." Toulouse : INP Toulouse, 2008. http://ethesis.inp-toulouse.fr/archive/00000578.

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Liu, Kun. "Catalytic Asymmetric Synthesis of Chiral Cyclic Amines and Axially Chiral Anilides by Phase-Transfer Catalyzed Reactions." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/158098.

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Soper, Jake D. "Reactions at nitrogenous ligands on oxidizing group 8 metal centers /." Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/8589.

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Devault, Damien. "Approche spatio-temporelle de la contamination par les herbicides de pré-levée du biotope de la Garonne Moyenne." Toulouse, INPT, 2007. http://ethesis.inp-toulouse.fr/archive/00000578/.

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L'application au milieu naturel d'un protocole de dosage des herbicides dans le sédiment a permit de dresser une cartographie de la contamination des sédiments et des eaux de surface appariées par les produits phytosanitaires. Au travers de ce premier état de la contamination du biotope aquatique, l'étude identifiera et caractérisera les sites où la charge en pesticides est la plus élevée : dans un contexte urbain et dans les discontinuités majeures propices à l'accumulation du sédiment (barrages). Des investigations furent alors menées pour comparer l'activité biologique du sédiment à sa char
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Chou, Chun-Tzer. "Part I, reaction of quinone imine monoketals with organolithium reagents. ; Part II, preparation of quinone imide monoketals by anodic oxidation of anilides. ; Part III, construction of the erythrina alkaloids skeleton /." The Ohio State University, 1987. http://rave.ohiolink.edu/etdc/view?acc_num=osu14875846121632.

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Jbarah, Abdel Aziz. "Spectroelectrochemistry of Substituted Anilines." Doctoral thesis, Universitätsbibliothek Chemnitz, 2006. http://nbn-resolving.de/urn:nbn:de:swb:ch1-200601985.

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Die Elektrochemie und die Spektroelektrochemie von Nitroanilinen (ortho-, meta- und para- Isomere) und deren entsprechenden Diaminoverbindungen (ortho-, meta- und para-Phenylendiamin) wurden an zwei verschiedenen Elektroden (Platin und Gold) und in zwei Elektrolytlösungen (saure und neutrale Perchloratlösung) untersucht. Die erhaltenen Messergebnisse wurden als Referenz für die spektroelektrochemische Untersuchung von Polyvinylaminen mit o- oder p- Nitroanilinsubstituenten verwendet. Es wurden außerdem spektroelektrochemische Untersuchungen mit anderen Polyvinylaminen, die das Wurster Kationra
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Books on the topic "Anilides"

1

SA, Helsinn, ed. Prostaglandins, oxidants and histamine in inflammation: A role for nimesulide? : augmented proceedings of a symposium held in Lugano, Switzerland, 30 November 1990. Adis International Ltd., 1991.

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Rappoport, Zvi, ed. The Chemistry of Anilines. John Wiley & Sons, Ltd, 2007. http://dx.doi.org/10.1002/9780470871737.

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Zvi, Rappoport, ed. The chemistry of anilines. Wiley, 2007.

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Canada, Canada Environment Canada, and Canada Health Canada, eds. Aniline. Environment Canada, 1994.

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I, Boeckhout C., Netherlands. Directoraat-Generaal van de Arbeid., and TAUW Infra Consult bv, eds. Werkterreinanalyse van aniline. Directoraat-Generaal van de Arbeid van het Ministerie van Sociale Zaken en Werkgelegenheid, 1991.

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Zok, Sabine. Metabolismus substituierter Aniline beim Zebrabärbling. [s.n.], 1991.

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Great Britain. Health and Safety Executive., ed. Aniline: Risk assessment document EH72/8. HSE Books, 1997.

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United States. Agency for Toxic Substances and Disease Registry. and Research Triangle Institute, eds. Toxicological profile for methylenedianiline. U.S. Dept. of Health and Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry, 1998.

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Syracuse Research Corporation. Center for Chemical Hazard Assessment. Monograph on human exposure to chemicals in the workplace : aniline: Final report. National Cancer Institute, Division of Cancer Etiology, 1985.

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National Institute for Occupational Safety and Health, ed. Morton International Chemical Company, Patterson [i.e. Paterson], New Jersey. U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1994.

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Book chapters on the topic "Anilides"

1

Gooch, Jan W. "Anilides." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_643.

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Johnson, Adam R., Christopher C. Cummins, and Sandro Gambarotta. "N-Tert -Alkyl-anilides as Bulky Anciliary Ligands." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132630.ch20.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 3 - Case 39 Periodinane-Mediated Cyclization of Anilides." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_39.

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Lide, David R. "Aniline." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-18.

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Gooch, Jan W. "Aniline." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_644.

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Patnaik, Pradyot. "Aniline." In Handbook of Environmental Analysis. CRC Press, 2017. http://dx.doi.org/10.1201/9781315151946-69.

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Gooch, Jan W. "Aniline Dye." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_646.

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Gooch, Jan W. "Aniline Ink." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_649.

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Gooch, Jan W. "Aniline Number." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_650.

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Gooch, Jan W. "Aniline Pigments." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_651.

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Conference papers on the topic "Anilides"

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Haskaj, Adelina, Musaj Pacarizi, Sonja Lepitkova, Berat Sinan, Bahri Sinani, and Elida Dreshaj. "THE POTENTIAL COMPLEXING IMPACT OF SOME ORGANIC COMPOUNDS AMINE AND CARBOXYL GROUPS ON TRANSITION METALS." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s18.42.

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Environmental water chemistry is substantially aided by modern electrochemical research. Sensitive voltammetric techniques are much more useful for metal species in natural waters, where complexation with organic molecules predominates. Many environmental electrochemists are still interested in determining the stability constants of metal ion complexes with various ionic species found in natural waterways. The aim of this work is to investigate the possible influence of complexation of amine and carboxyl groups of some organic molecules (with EDTA, NTA and aniline, using differential pulse pol
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Sterczewski, Lukasz A., Jakub Mnich, and Jaroslaw Sotor. "Multi-Octave THz Generation and Detection at MHz Repetition Rates using the Organic Nonlinear Crystal PNPA." In CLEO: Science and Innovations. Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_si.2024.sm2p.5.

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Generation and detection of broadband THz radiation using the PNPA ((E)-4-((4-nitrobenzylidene)amino)-N-phenyl-aniline) crystal at MHz repetition rates is demonstrated. Compatibility with nanojoule pump pulses at telecommunication wavelengths makes this medium attractive for compact THz spectrometers.
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Jauhari, Smita, and Bhupendra Mistry. "“Study of the Inhibitive Effect of Novel Quinoline Schiff Base on Corrosion of Mild Steel in HCl Solution”." In CORROSION 2013. NACE International, 2013. https://doi.org/10.5006/c2013-02326.

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Abstract Schiff base 4-Chloro-N-[(2-chloroquinolin-3-yl)methylene]aniline was synthesized, and its inhibitive effect for mild steel in 1M HCl solution was investigated by weight loss measurement and electrochemical tests.From the weight loss measurements and electrochemical tests, it was observed that the inhibition efficiency increases with the increase in the Schiff base concentration and reaches a maximum at the optimum concentration. This is further confirmed by the decrease in corrosion rate. It is found that the system follows Langmuir adsorption isotherm.
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Jauhari, Smita, and Bhupendra Mistry. "Study of the Inhibitive Effect of Novel Schiff Base on Corrosion of HCL on Mild Steel." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01478.

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Abstract Schiff base (E)-3-chloro-N-((2-chloroquinolin-3-yl)methylene)aniline (CQA) was synthesized, and its inhibitive effect for mild steel in 1M HCl solution was investigated by weight loss measurement and electrochemical tests. From the weight loss measurements and electrochemical tests, it was observed that the inhibition efficiency increases with the increase in the Schiff base concentration and reaches a maximum at the optimum concentration. This is further confirmed by the decrease in corrosion rate. It is found that the system follows Langmuir adsorption isotherm.
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Omotosho, Olugbenga Adeshola, Joshua Olusegun Okeniyi, and Abimbola Patricia Idowu Popoola. "Corrosion Inhibition of Stainless Steel in 0.5 M HCl by C6H5NH2." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-10807.

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Abstract In this study, different concentrations of C6H5NH2 (Aniline) were employed for investigating its corrosion inhibition of stainless steel in 0.5 M HCl. Corrosion rate measurements at 28°C, 45°C and 60°C were obtained from a linear sweep voltametry instrument and analyzed for inhibition efficiency and apparent activation energy in the presence and absence of C6H5NH2. Results showed that C6H5NH2 generally exhibited excellent inhibition effects on stainless steel corrosion at the higher temperatures, i.e. the 45°C and 60°C, at which the self-protectiveness of the stainless steel metal app
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Li, Jie, Boya Zhang, Xuanjie Zhang, Yixuan Li, Xiao Yuan, and Xingwen Li. "Effect of Large Linking Groups on the Electrical and Thermal Properties of Aniline Cured Epoxy Resins." In 2024 3rd International Conference on Power Systems and Electrical Technology (PSET). IEEE, 2024. https://doi.org/10.1109/pset62496.2024.10808806.

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Bobal, Pavel, Josef Jampilek, Jan Otevrel, and Josef Sujan. "Microwave-assisted synthesis of new substituted anilides of quinaldic acid." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00681.

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Dolezal, Martin, Miroslav Miletin, Jiri Hartl, Katarina Kralova, and Jiri Kunes. "Synthesis of Some Anilides of Substituted Pyrazine-2-carboxylic Acids and Their Photosynthesis-inhibiting Activity." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01921.

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Kon, Yoshihiro. "Selective monoallylation of anilines to form fine chemicals using allyl alcohol derived from glycerol." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/mjrr3569.

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Glycerol is an important starting material for the production of value-added chemicals such as electronic materials and pharmaceuticals. We herein present a selective allylation reaction using allyl alcohol which is given from glycerol. First, we show the rhenium catalyzed high-yielding synthesis of allyl alcohol from glycerol through deoxydehydration reaction. Next, the selective N-allyl aniline synthesis from allyl alcohol with aniline is performed. The well-dispersed tungsten oxide supported on zirconium oxide can catalyze the reaction to produce the corresponding mono-allyl compound over
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Miletin, Miroslav, Martin Dolezal, Jiri Hartl, Katarina Kralova, and Milos Machacek. "Synthesis of some anilides of 2-alkylsulfanyl- and 2-chloro-6-alkylsulfanyl-4-pyridinecarboxylic acids and their photosynthesis-inhibiting activity." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01767.

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Reports on the topic "Anilides"

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Feng, J., W. Zhang, A. G. MacDiarmid, and A. J. Epstein. Synthesis and Characterization of Oligomeric Anilines. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada330138.

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Zhou, H. C., and R. S. Duran. The Effect of Surface Pressure on Langmuir-Blodgett Polymerization of 2- Pentadecyl Aniline. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada250993.

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Bernstein, E. R., M. F. Hineman, S. K. Kim, and D. F. Kelley. Vibrational Dynamics of Aniline (N2)1 Clusters in Their First Excited Singlet State. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada245812.

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Huang, S. X., J. L. Gland, and D. A. Fischer. Aniline hydrogenolysis on the Pt(111) single crystal surface: Mechanisms for C-N bond activation. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10117539.

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Essington, M. E., J. M. Bowen, R. A. Wills, and B. K. Hart. Adsorption of aniline and toluidines on montmorillonite: Implications for the disposal of shale oil production wastes. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6745527.

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Essington, M. E., J. M. Bowen, R. A. Wills, and B. K. Hart. Adsorption of aniline and toluidines on montmorillonite: Implications for the disposal of shale oil production wastes. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10133217.

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Ruangpornvisuti, Vithaya. Basicity investigation and structure optimization of polyaza-Calixarenes and stabilities of their complexes with metal cations. Chulalongkorn University, 2000. https://doi.org/10.58837/chula.res.2000.26.

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The structure of 25, 26, 27, 28-tetra(2-ethoxyaniline)calix[4]arene of cone (cL) and partial cone (pcL) conformations were optimized by PM3 of quantum chemical method. It has been found that cL structure is more stable than pcL conformation. The stabilization energies of protonation on four aniline-nitrogen atoms of both conformations of the ligand at 6-31G energy level, were obtained. The protonations process on the cL and pcL being 7 and 24 possible pathways, respectively, were evaluated. The basicity constants of partial cone conformation of 25, 26, 27, 28-tetra(2- ethoxyaniline)calix[4]are
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NIOSH skin notation (SK) profile: aniline [CAS No. 62-53-3]. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 2015. http://dx.doi.org/10.26616/nioshpub2015192.

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Request for assistance in preventing bladder cancer from exposure to o-toluidine and aniline. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control, National Institute for Occupational Safety and Health, 1990. http://dx.doi.org/10.26616/nioshpub90116.

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