Relevant bibliographies by topics / Synthetic derivatives

Contents

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

Academic literature on the topic 'Synthetic derivatives'

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

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Journal articles on the topic "Synthetic derivatives"

1

Petrini, Marino, and Alessandro Palmieri. "Recent Advances in the Synthesis of Unsymmetrical Bisindolylmethane Derivatives." Synthesis 51, no. 04 (2018): 829–41. http://dx.doi.org/10.1055/s-0037-1610349.

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This review article summarizes the fundamental synthetic procedures aimed at the preparation of unsymmetrical bisindolylmethanes that have appeared in the literature since 2010. To this goal, reactive electrophilic indole-containing intermediates are mostly generated from indolylmethanols, indolylmethanamines, and indolylmethanthio derivatives and then made to react with simple or functionalized indoles. The asymmetric synthesis of bisindolylmethanes can be also achieved under chiral-catalyzed conditions.1 Introduction2 Direct Three-Component Coupling3 Reaction of Indolylmethanols4 Reaction of
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Jurczak, Janusz, Agnieszka Cholewiak, and Pawel Stepniak. "Linear Neutral Receptors for Anions: Synthesis, Structure and Applications." Synthesis 50, no. 23 (2018): 4555–68. http://dx.doi.org/10.1055/s-0037-1609943.

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A selective digest of linear anion receptors based on different aromatic skeletons is presented. Since the structures of anions vary from one to another, different strategies have been developed over recent years in order to bind anions efficiently and selectively. Rigidity, number of hydrogen bond donors, steric hindrance, and special preorganization of linear receptors are analyzed to shed light on the rational design of anion receptors.1 Introduction2 1,3- and 1,2-Benzene Derivatives3 1,3- and 5,7-Azulene Derivatives4 1,8-Naphthalene Derivatives5 1,8-Anthracene Derivatives6 2,6-Pyridine Der
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Kumar, Akhalesh, Rakhi Mishra, Avijit Mazumder, Rupa Mazumder, and Arun Kumar. "An Updated Review on Synthesis and Biological Activities of Thiosemicarbazide Analogs." Asian Journal of Chemistry 33, no. 9 (2021): 1957–75. http://dx.doi.org/10.14233/ajchem.2021.23218.

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This review paper focuses on the different synthetic methodologies that researchers have adopted to synthesize various thiosemicarbazide derivatives with different biological activities of synthesized compounds in the last 20 years. Most of the investigations available in the literature are directed to the biological activities of thiosemicarbazide derivatives with less discussion on its synthetic schemes. This review article presents various reaction scheme, which has been adopted for thiosemicarbazide derivative synthesis along with the reported pharmacological activities of synthesized anal
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Smolobochkin, Andrey V., Almir S. Gazizov, Rakhymzhan A. Turmanov, Dinara S. Abdullaeva, Alexander R. Burilov, and Michail A. Pudovik. "N-Phosphorylated Pyrrolidines: An Overview of Synthetic Approaches." Synthesis 52, no. 15 (2020): 2162–70. http://dx.doi.org/10.1055/s-0039-1690889.

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Organophosphorus pyrrolidine derivatives possessing P–N bonds are a promising yet underexplored class of compounds. In this short review we overview the general approaches to these compounds described so far, with a special emphasis on their asymmetric synthesis.1 Introduction2 Synthesis of Pyrrolidine-Based P(III) Derivatives3 Synthesis of Pyrrolidine-Based P(V) Derivatives3.1 Phosphorylation of Pyrrolidines with P(V) Acid Chlorides3.2 Phosphorylation of Pyrrolidines with P(V) Acid Esters3.3 Syntheses via the Atherton–Todd Reaction3.4 Oxidation of Pyrrolidine-Based P(III) Derivatives4 Synthes
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Xie, Yang, Zhou Xu, Pei Hu, et al. "Synthesis of the Isodityrosine Moiety of Seongsanamide A–D and Its Derivatives." Marine Drugs 21, no. 7 (2023): 373. http://dx.doi.org/10.3390/md21070373.

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The concise and highly convergent synthesis of the isodityrosine unit of seongsanamide A–D and its derivatives bearing a diaryl ether moiety is described. In this work, the synthetic strategy features palladium-catalyzed C(sp3)–H functionalization and a Cu/ligand-catalyzed coupling reaction. We report a practical protocol for the palladium-catalyzed mono-arylation of β-methyl C(sp3)–H of an alanine derivative bearing a 2-thiomethylaniline auxiliary. The reaction is compatible with a variety of functional groups, providing practical access to numerous β-aryl-α-amino acids; these acids can be co
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Sato, Ken-ichi, Shoji Akai, and Juji Yoshimura. "Stereocontrolled Total Synthesis of Tetrodotoxin from myo-Inositol and D-Glucose by Three Routes: Aspects for Constructing Complex Multi-Functionalized Cyclitols with Branched-Chain Structures." Natural Product Communications 8, no. 7 (2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800726.

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This report describes the stereocontrolled total synthesis of the multi-functionalized cyclitol derivative tetrodotoxin containing eight asymmetric carbons and different types of branched-chains from myo-inositol and D-glucose using three different methods. The tetrodotoxin derivatives possess a relatively small molecular weight but unique structural and chemical properties. Selection of the appropriate synthetic method may be useful not only for compounds related to TTX (including related derivatives) but also for other highly complex multi-functionalized cyclitols containing branched-chains.
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Sato, Ken-Ichi, Shoji Akai, and Juji Yoshimura. "Stereocontrolled Total Synthesis of Tetrodotoxin from myo-Inositol and D-Glucose by Three Routes: Aspects for Constructing Complex Multi-Functionalized Cyclitols with Branched-Chain Structures." Natural Product Communications 10, no. 5 (2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000501.

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This report describes the stereocontrolled total synthesis of the multi-functionalized cyclitol derivative, tetrodotoxin, containing eight asymmetric carbons and different types of branched-chains, from myo-inositol and D-glucose using three different methods. The tetrodotoxin derivatives possess a relatively small molecular weight but unique structural and chemical properties. Selection of the appropriate synthetic method may be useful not only for compounds related to TTX (including related derivatives), but also for other highly complex multi-functionalized cyclitols containing branched-cha
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Kanazawa, Junichiro, and Masanobu Uchiyama. "Recent Advances in the Synthetic Chemistry of Bicyclo[1.1.1]pentane." Synlett 30, no. 01 (2018): 1–11. http://dx.doi.org/10.1055/s-0037-1610314.

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Utilization of three-dimensional cyclic scaffolds is important in modern drug discovery, both to provide greater opportunities for optimizing drug candidates and to expand the available chemical space of drugs. Among these scaffolds, bicyclo[1.1.1]pentane (BCP) is a high-value bioisostere for 1,4-disubstituted phenyl rings, internal alkynes, and the tert-butyl group, generally offering high passive permeability, high water solubility, and improved metabolic stability. However, the lack of methods for functionalizing BCP remains a significant challenge, and in particular, a versatile strategy f
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Tschakert, Jochen, and Wolfgang Voelter. "Festphasensynthese von Muramyldipeptidderivaten und Untersuchung ihrer biologischen Aktivität / Solid Phase Synthesis of Muramyl Dipeptide Derivatives and Investigations on their Biological Activities." Zeitschrift für Naturforschung B 49, no. 5 (1994): 702–16. http://dx.doi.org/10.1515/znb-1994-0524.

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New muramyl dipeptide derivatives with exchanged carbohydrate residues are described. Each derivative is synthesized via a solid phase synthesis using an aminomethyl anchor resin. All synthetic products can be isolated in good yields. Their biological activities are tested by the luminol-dependent chemiluminescence associated with the phagocytosis of opsonized zymosan by granulocytes.
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LÓPEZ LÓPEZ, Lluvia Itzel, Sendar Daniel NERY FLORES, Sonia Yesenia SILVA BELMARES, and Aidé SÁENZ GALINDO. "Naphthoquinones: biological properties and synthesis of lawsone and derivates - a structured review." Vitae 21, no. 3 (2014): 248–58. http://dx.doi.org/10.17533/udea.vitae.17322.

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Background: Naphthoquinones are natural pigments that are widely distributed in nature and have important biological activities. Lawsone (2-hydroxy-1,4-naphthoquinone) and its synthetic derivatives, and especially those containing nitrogen, have promising potential for the treatment of different diseases due to their antibacterial, antifungal, antiviral, antitumor and antiparasitic effects, and for pest control via their molluscicidal and insecticidal activities. Their pharmacological activities and mechanisms of action are related to their oxide/reduction and acid/base properties, and can be
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Dissertations / Theses on the topic "Synthetic derivatives"

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Stockmann, Vegar. "Synthetic Applications of Nitropyridine Derivatives." Doctoral thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for kjemi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-12220.

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The present work represents a continuation of the investigation of the chemistry of nitropyridine derivatives, based on the methodology for nitration of pyridines developed by Professor Jan M. Bakke and co-workers at NTNU. Nitropyridines have been utilized as substrates for the formation of novel bis- and tris-heterocyclic compounds, and new synthetic routes to fused heterocycles have been developed. Several new β-carboline analogues and fused azacinnolines have been prepared based on a Suzuki coupling and subsequent cyclization approuch. The formation of 4-isocyanobut-2-enenitrile and 3-cyano
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Karim, Rehana. "Development of radical synthetic methodology using solid-phase organic synthesis." Thesis, Loughborough University, 2003. https://dspace.lboro.ac.uk/2134/34406.

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The synthesis of heterocycles using radical intermediates has become an important area of research in recent years. The aim of our research was to develop radical methodologies to construct heterocycles on solid-support. Tri-cyclic benzimidazole derivatives are desirable synthetic targets with a range of biological activity and are part of certain anti-tumour agents. Solid-supported radical reactions with substituted benzimidazoles were performed under different experimental conditions, including different solvents, three different resins (Wang, Merrifield and Rink) and different radical reage
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Navasero, Neenah. "Synthetic routes to non-symmetric tropones." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=101647.

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The synthesis of substituted non-symmetric tropones has proven to be a considerable synthetic challenge. Particularly, a 3,4,6-tnsubstituted tropone which is required for the total synthesis of CP-225,917 is currently being undertaken by our group.<br>Two approaches towards the synthesis of substituted tropones are presented. Both utilize linear diene precursors which are closed to 7-membered cycloheptene rings via ring closing metathesis. In the first method, linear precursors are synthesized by addition of nucleophilic substituents to carbonyl groups to form alcohol groups. After forming the
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Howarth, Nicola. "Synthetic approaches to derivatives of tropane." Thesis, University of Leicester, 1991. http://hdl.handle.net/2381/33742.

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This thesis is a continuation of the work by Bathate, which had shown that intramolecular cyclisation of trans-1- (benzylamino)-4-chlorocycloheptane and hept-2-ene gave the corresponding nortropane and nortrop-6-ene derivatives. Problems were experienced in the reproducibility of Bathgate's route. Therefore, the intramolecular cyclisation step warranted further development. The best yields of cyclised products were attained when the solvent was changed to acetone. Other approaches to nortropane were sought. Reasonable yields of the cyclised material were only obtained when the nitrogen functio
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Stewart, Alistair J. "Synthetic studies in nucleoside chemistry." Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.232863.

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Bode, Moira Leanne. "Synthetic and spectroscopic studies of indolizine derivatives." Thesis, Rhodes University, 1994. http://hdl.handle.net/10962/d1005050.

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The crystalline compound resulting from thermal cyclization of the Baylis-Hillman product, methyl 3-hydroxy-2-methylene-3-(2-pyridyl)propanoate, has been identified as the indolizine derivative, methyl indolizine-2-carboxylate, and this approach involving the reaction of pyridine-2-carboxaldehydes and acrylate analogues has been established as a general route to 2-substituted indolizines. The ease of cyclization the Baylis-Hillman products to indolizines has been shown to increase by converting the hydroxy group to an acetoxy group, and a range of acetylated Baylis-Hillman products were prepar
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Gelebe, Aifheli Carlson. "Synthetic and spectrometric studies of benzodioxepinone derivatives." Thesis, Rhodes University, 1995. http://hdl.handle.net/10962/d1005047.

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An extensive range of oxygen and sulphur substituted benzodiazepine analogues has been synthesised via Baeyer-Villiger and Schmidt reactions of specially prepared flavanone and N-acetyl-4-quinolone precursors. Alternative, cyclisation routes have also been used to prepare some of these compounds. Ring-opening reactions of 1,5-benzodioxepinones have been investigated and a detailed kinetic-mechanistic study of the Baeyer-Villiger reaction of flavanones has been carried out using 1 H NMR spectroscopy to explain the observed regiochemistry of oxygen insertion. The electron-impact mass spectrometr
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Lobb, Kevin Alan. "Camphor derivatives in asymmetric synthesis: a synthetic, mechanistic and theoretical study." Thesis, Rhodes University, 2008. http://hdl.handle.net/10962/d1006770.

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A series of 3,3-ethylenedioxy-exo- and endo- bornyl esters have been prepared and subjected to α-benzylation using lithium diisopropylamide and benzyl bromide. In the exo-series of esters the diastereofacial selectivity of benzylation was found to improve (up to 34% d.e.) as the steric bulk of the O-alkyl group increased, whereas in the endo-series, a surprising decrease in stereoselectivity was observed as the steric bulk increased – an observation attributed to flexibility of the metal-coordinated endo-enolate system, compared to the relative rigidity of the exo analogues. The conformational
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Lilley, Ian Andrew. "Synthetic studies using chiral stabilised azomethine ylids." Thesis, University of Oxford, 1995. https://ora.ox.ac.uk/objects/uuid:64d5745b-e6ef-4a77-8abe-b01f1c627e8f.

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The work described herein is concerned with the [3+2] dipolar cycloaddition of amino acid derived azomethine ylids. Such cycloadditions are a highly efficient technique for the construction of proline derivatives, and may potentially be employed in other areas of asymmetric synthesis. Chapter 1 commences with a brief review of natural and synthetic, proline containing, molecules. Approaches to the synthesis of the proline moiety are described, focusing on previously developed methods for performing the [3+2] dipolar cycloaddition in a chiral manner. The methodology employed in this thesis is s
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Langnel, David Antoine Fernand. "New synthetic routes to antitumour imidazotetrazines." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311742.

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Books on the topic "Synthetic derivatives"

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Choudhry, Moorad. Structured credit products: Credit derivatives and synthetic securitisation. Wiley & Sons (Asia), 2004.

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M, Tavakoli Janet, ed. Credit derivatives & synthetic structures: A guide to instruments and applications. 2nd ed. Wiley, 2001.

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Tekle-Smith, Makeda Aislinn. Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development. [publisher not identified], 2019.

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Mary, Cebulak, ed. Cyclitols and their derivatives: A handbook of physical, spectral, and synthetic data. VCH Publishers, 1993.

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Wardell, Ian. Heterodiene cycloadditions of enoic acid derivatives: Synthetic scope and limitations. University of Salford, 1989.

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Howe, Steven D. A synthetic, spectroscopic and conductometric study of some phthalocyanine derivatives. University ofEast Anglia, 1986.

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Rubiralta, Mario. Piperidine: Structure, preparation, reactivity, and synthetic applications of piperidine and its derivatives. Elsevier, 1991.

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Веселков, Алексей Никонович, and Alexei N. Veselkov. Anti-cancer drug design: Biol. a. biophys. aspects of synthetic phenoxazone derivatives. SEVNTU press, 2002.

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Jokela, Reija. Indolo(2.3-a)quinolizine and n-methylpiperidine derivatives: Synthetic methods and stereochemical considerations. Suomalainen Tiedeakatemia, 1985.

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Cremins, Peter John. Synthetic transformations of 4-Oxo-4H-1-Benzopyran derivatives and approaches to anthracycline analogues. University of Salford, 1986.

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Book chapters on the topic "Synthetic derivatives"

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Backinowsky, L. V. "Sugar Cyanoethylidene Derivatives." In Synthetic Oligosaccharides. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0560.ch003.

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Nishihara, Ryo, Daniel Citterio, and Koji Suzuki. "Synthetic Bioluminescent Coelenterazine Derivatives." In Bioluminescence. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3813-1_2.

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Lancaster, Brian P., and Anthony G. Butler. "Synthetic CRE CDOs." In Structured Products and Related Credit Derivatives. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119197836.ch16.

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McManus, Brian, Steven Todd, Dave Preston, and Anik Ray. "Credit Derivatives and Synthetic CDOs." In Structured Products and Related Credit Derivatives. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119197836.ch11.

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Cai, Chao, Jun Li, Fei Fan, Guoyun Li, Chunxia Li, and Guangli Yu. "CHAPTER 12. Synthesis of Marine Polysaccharides/Oligosaccharides and Their Derivatives." In Synthetic Glycomes. Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788016575-00281.

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Gulevich, Anton V., Alexander G. Zhdanko, Romano V. A. Orru, and Valentine G. Nenajdenko. "Synthetic Application of Isocyanoacetic Acid Derivatives." In Isocyanide Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527652532.ch4.

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Morales, Paula, and Nadine Jagerovic. "Synthetic and Natural Derivatives of Cannabidiol." In Advances in Experimental Medicine and Biology. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-61663-2_2.

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Bielski, Roman, and Zbigniew J. Witczak. "Novel Levoglucosenone Derivatives." In Domino and Intramolecular Rearrangement Reactions as Advanced Synthetic Methods in Glycoscience. John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119044222.ch11.

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Ohno, Hiroaki, Norihito Arichi, and Shinsuke Inuki. "Nonbiomimetic Total Synthesis of Polycyclic Alkaloids." In Modern Natural Product Synthesis. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1619-7_19.

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AbstractIn nonbiomimetic natural product synthesis, there are no restrictions on the design of synthetic routes; however, the feasibility of the planned routes is often completely unknown. To discover more efficient and creative syntheses of natural products, and to identify bioactive natural product derivatives that have never been synthesized in nature, our group is engaged in the nonbiomimetic total synthesis of indole alkaloids. In this chapter, we describe our nonbiomimetic total syntheses of quinocarcin, dictyodendrins A–F, and zephycarinatines C and D, by employing alkyne-based approach
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Hasegawa, Akira. "Synthesis of Sialo-oligosaccharides and Their Ceramide Derivatives as Tools for Elucidation of Biologic Functions of Gangliosides." In Synthetic Oligosaccharides. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0560.ch011.

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Conference papers on the topic "Synthetic derivatives"

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Artiukh, Liubov, Olga Povnitsa, Yuriy Shermolovich, Sergiy Siry, and Svitlana Zahorodnia. "The Antiviral Activity of Trifluoromethylthiolane Derivatives." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13643.

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Munín, Javier, Dolores Viña, Lourdes Santana, Eugenio Uriarte, and Elías Quezada. "Synthesis of new phthalazinedione derivatives." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00664.

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Cabrera-Escribano, F., M. Gómez-Guillén, P. Borrachero, I. Vázquez-Férnandez, S. Jatunov, and A. Franconetti. "New fluorescent amino carbohydrate derivatives." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00695.

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Oliveira-Campos, Ana, césar Bernardo, Ana Olival, António Ribeiro, Lígia Rodrigues, and Ana Esteves. "Synthesis of B-carboline Derivatives." In The 16th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-00997.

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Uchida, T., K. Kozawa, Y. Kimura, and Y. Goto. "Structural study of chalcone derivatives." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835970.

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Pino-Gonzalez, M. Soledad, and Inmaculada Martin-Torres. "Benzimidazoles from D-glucose derivatives." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a066.

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Baba-Ahmed, Ikram, Zahira Kibou, Julio A. Seijas, et al. "Pyridine Derivatives as Fluorescent Sensors for Cations." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16086.

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Missoum, Hadjer, Yazid Datoussaid, Noureddine Choukchou-braham, Julio A. Seijas, and Maria Pilar Vázquez-Tato. "Synthesis and Reactivity of 2-Acetylthiophenes Derivatives." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16132.

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Cabrera, José, Mateo Alajarín, and Aurelia Pastor. "Dimeric Anhydro Bases from Benzothiazole Derivatives." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01402.

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Ha, Sie-Tiong, Peng-Lim Boey, and Guan-Yeow Yeap. "Mesomorphic properties of new cholesteryl derivatives." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00386.

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Reports on the topic "Synthetic derivatives"

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Banks, H. D., D. F. Taber, and P. B. Deker. Metabolites of the Fentanyl Family. Synthetic Studies on the 3-Hydroxy Derivatives. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada212730.

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Archibald, T. G., M. Farnia, and K. Baum. Synthesis of Tetra-Functional Cubane Derivatives. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada205919.

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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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Hart, Carl, Gregory Lyons, and Michael White. Spherical shock waveform reconstruction by heterodyne interferometry. Engineer Research and Development Center (U.S.), 2024. http://dx.doi.org/10.21079/11681/48471.

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The indirect measurement of shock waveforms by acousto-optic sensing requires a method to reconstruct the field from the projected data. Under the assumption of spherical symmetry, one approach is to reconstruct the field by the Abel inversion integral transform. When the acousto-optic sensing modality measures the change in optical phase difference time derivative, as for a heterodyne Mach–Zehnder interferometer, e.g., a laser Doppler vibrometer, the reconstructed field is the fluctuating refractive index time derivative. A technique is derived that reconstructs the fluctuating index directly
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Renn, Julia. Synthesis and Characterization of Novel SF5 Containing Fluoroalkyl Iodides and Derivatives. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.7182.

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Parshikov, I. A. Synthesis of Biosafe Hydroxy Derivatives of the Potentially Antitumor Drug Artemisinin by Basidiomycetes. Russian Scientific Journal, 2018. http://dx.doi.org/10.18411/1995-4417n3_2018.

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Schubert, David M., Mark J. Manning, and M. F. Hawthorne. The Synthesis and Structural Characterization of Carborane Derivatives Containing Main Group and F-Block Elements. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada239151.

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Holcomb, Nelson. Synthesis and Characterization of Novel Fluorine Containing Alkylsulfonyls and Sulfonates : Fluorinated Sulfonyl Methanes and Derivatives. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.6931.

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Shafii, B., R. W. Atcher, and E. R. DeSombre. An improved and facile method for the synthesis of 1,1-bis(4-hydroxyphenyl)-2-phenylethylene and its derivatives. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10188496.

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Hemscheidt, Thomas. Semi-Synthesis and In-Vitro Anticancer Evaluation of Derivatives of a New Microtubule Poison with a Taxol-Like Mechanism. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada411590.

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