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Relevant bibliographies by topics / Heterocyclic chemistry

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Academic literature on the topic 'Heterocyclic chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 30 July 2024

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Journal articles on the topic "Heterocyclic chemistry"

1

Andres, C. J., Derek J. Denhart, Milind S. Deshpande, and Kevin W. Gillman. "Recent Advances in the Solid Phase Synthesis of Drug Heterocyclic Small Molecules." Combinatorial Chemistry & High Throughput Screening 2, no. 4 (August 1999): 191–210. http://dx.doi.org/10.2174/1386207302666220204193145.

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Abstract: Because of their synthetic challenge, broad range of physical I chemical properties, and diverse biological activities, heterocycles continue to be of interest to both the academic and industrial chemist. This review covers recent advances in the solid phase synthesis of drug-like heterocyclic small molecules. Syntheses which form the heterocycle on the solid phase are emphasized; syntheses in which a preformed heterocycle is functionalized on the solid support have been omitted. The majority of references are from publication year 1999. This review should be of interest to anyone involved in, or contemplating the solid phase synthesis of small molecule drug-like heterocycles, especially for combinatorial chemistry applications.

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Luna, Isadora Silva, Rayssa Marques Duarte da Cruz, Ryldene Marques Duarte da Cruz, Rodrigo Santos Aquino de Araújo, and Francisco Jaime Bezerra Mendonça-Junior. "1,4-Dithiane-2,5-diol: A Versatile Synthon for the Synthesis of Sulfur-containing Heterocycles." Current Organic Synthesis 15, no. 8 (December 17, 2018): 1026–42. http://dx.doi.org/10.2174/1570179415666180821154551.

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Background: 1,4-Dithiane-2,5-diol (1,4-DTD) is the stable dimer of α-mercapto acetaldehyde. This commercially available ambidentade compound is characterized as having in its chemical structure one group that acts as an electrophile and another that acts as a nucleophile, this permits its use as versatile and efficient synthon in synthetic heterocycle procedures. Objective: The aim of this review is to present synthetic applications of 1,4-DTD in heterocyclic chemistry and their applicability to the synthesis of bioactive compounds. Conclusion: Gewald reactions to obtain C-4 and C-5 unsubstituted 2-amino-thiophene derivatives; sulfa- Michael/Henry and sulfa-Michael/aldol sequences to obtain polysubstituted tetrahydrothiophenes, and other heterocyclic reactions that allow synthesizing several functionalized sulfur-containing heterocycles such as thiazolidines, oxathiazinoles and thiazoles are presented and discussed. The use of such heterocyclics in subsequent reactions allows obtaining various bioactive compounds including the antiretroviral lamivudine which is one of the examples presented in this review.

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Romero-Hernández, Laura L., Ana Isabel Ahuja-Casarín, Penélope Merino-Montiel, Sara Montiel-Smith, José Luis Vega-Báez, and Jesús Sandoval-Ramírez. "Syntheses and medicinal chemistry of spiro heterocyclic steroids." Beilstein Journal of Organic Chemistry 20 (July 24, 2024): 1713–45. http://dx.doi.org/10.3762/bjoc.20.152.

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There is compelling evidence that incorporating a heterocyclic moiety into a steroid can alter its pharmacological and pharmacokinetic properties, driving intense interest in the synthesis of such hybrids among research groups. In this review, we present an overview of recent synthetic methodologies, spanning the period from 2000 to 2023, for the preparation of spiro heterocyclic steroids. The compounds surveyed encompass four-, five-, six-, and seven-membered heterocycles appended to various positions of steroidal backbones, with spirocycles containing oxygen, nitrogen, and sulfur atoms being predominant. The outlined synthetic procedures emphasize the pivotal steps for constructing the heterocycles, often accompanied by a detailed account of the overall synthesis pathway. The review encompasses innovative compounds, including bis-steroids linked by a spiro heterocycle and steroids conjugated to heterocyclic moieties containing three or more (hetero)cycles. Moreover, many compounds are accompanied by data on their biological activities, such as antiproliferative, antimalarial, antimicrobial, antifungal, steroid antagonist, and enzyme inhibition, among others, aimed at furnishing pertinent insights for the future design of more potent and selective drugs.

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Charushin, V. N., E. V. Verbitskiy, O. N. Chupakhin, D. V. Vorobyeva, P. S. Gribanov, S. N. Osipov, A. V. Ivanov, et al. "The chemistry of heterocycles in the 21st century." Russian Chemical Reviews 93, no. 7 (July 2024): RCR5125. http://dx.doi.org/10.59761/rcr5125.

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The chemistry of heterocyclic compounds has traditionally been and remains a bright area of chemical science in Russia. This is due to the fact that many heterocycles find the widest application. These compounds are the key structural fragments of most drugs, plant protection agents. Many natural compounds are also derivatives of heterocycles. At present, more than half of the hundreds of millions of known chemical compounds are heterocycles. This collective review is devoted to the achievements of Russian chemists in this field over the last 15–20 years. The review presents the achievements of leading heterocyclists representing both RAS institutes and university science. It is worth noting the wide scope of the review, both in terms of the geography of author teams, covering the whole of our large country, and in terms of the diversity of research areas. Practically all major types of heterocycles are represented in the review. The special attention is focused on the practical applications of heterocycles in the design of new drugs and biologically active compounds, high-energy molecules, materials for organic electronics and photovoltaics, new ligands for coordination chemistry, and many other rapidly developing areas. These practical advances would not be possible without the development of new fundamental transformations in heterocyclic chemistry.<br> Bibliography — 2237 references.

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Sharma, Praveen Kumar, Andleeb Amin, and M. Kumar. "Synthetic Methods of Medicinally Important Heterocycles-thiazines: A Review." Open Medicinal Chemistry Journal 14, no. 1 (September 14, 2020): 71–82. http://dx.doi.org/10.2174/1874104502014010071.

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Heterocyclic compounds containing N and S atoms have unique properties so that they can be used as potential reactive materials in pharmacokinetic systems. In medicinal chemistry, the therapeutic applications of nitrogen sulphur heterocycles are well known. Especially, Thiazines attract the attention of chemists due to their great bioactive behavior. The present study is a review of the work carried out by the research community for the synthesis of novel, effective, medicinally important heterocyclic compounds-thiazines.

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Bhattacharya, Somenath, Soumallya Chakraborty, Rohan Pal, Sourav Saha, Bhaskar Ghosh, Chiranjit Mandal, Dr Amitava Roy, and Dr Arin Bhattacharjee. "A Comprehensive Review on Pyrazole and It’s Pharmacological Properties." International Journal for Research in Applied Science and Engineering Technology 10, no. 9 (September 30, 2022): 1769–74. http://dx.doi.org/10.22214/ijraset.2022.46924.

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Abstract: Heterocyclic chemistry is very important aspects in organic chemistry. Heterocyclic system consists of one or more heteroatoms like nitrogen, oxygen, sulphur, etc with hydrogen atoms. The system can be classified as saturated as well as non saturated system or hydrocarbons. Another classification of this ring system is divided in some categories like three-membered, four-membered, five-membered, six-memebered, seven-membered, fused heterocyclics etc. Some compounds under this cklassification are acidic or basic in nature. Examples of heterocyclic compounds are Pyrole, Furan, Thiophene, Pyridine, Quinoline, Isoquinoline, Indole, Purine, Pyrazole, etc. Pyrazole is very important under this heterocyclic ring sysyem. Pyrazole is five membered heterocyclics. Pyrazole is basic and unsaturated in nature due to presence of double bonds in their ring structure. When two nitrogen atoms are associated with five menbered heterocyclic ring in 1,2 positions called as Pyrazole structure. It is also known as 1,2-diazole. It is present in many drugs as well as organic compounds and Pharmaceutical compounds. The review study shown that the structure, physical and chemical properties, nomenclature, synthetic approaches, biological activities of Pyrazole heterocyclic ring structure

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Georghiou, Paris E. "Preface." Pure and Applied Chemistry 82, no. 9 (January 1, 2010): iv. http://dx.doi.org/10.1351/pac20108209iv.

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The 22nd International Congress on Heterocyclic Chemistry (ICHC-22) was held 2-7 August 2009 in St. John's, Newfoundland and Labrador, Canada. St. John's, the capital of Canada's youngest Province, Newfoundland and Labrador, is also Canada’s oldest and North America’s most easterly city. The Conference was chaired by Prof. Mohsen Daneshtalab (School of Pharmacy, Memorial University of Newfoundland) and was organized by the School of Pharmacy and the Chemistry Department at Memorial University of Newfoundland.Approximately 260 participants from over 30 different countries attended. The scientific program consisted of 10 plenary lectures, 19 invited lectures, 52 short communications, and 115 posters. Prof. Samuel Danishefsky (Sloan-Kettering Institute for Cancer Research, Columbia University) was honored with the 2009 ISHC Senior Award in Heterocyclic Chemistry, and Prof. John Wood (Colorado State University) was the 2009 Katritzky Junior Award winner. A special symposium entitled "Focus on heterocycles in organic synthesis today and tomorrow" was held during the Congress as a tribute to Prof. Victor Snieckus (Queen's University, Kingston) for his research accomplishments and long-time contribution to the International Society of Heterocyclic Chemistry (ISHC).The five Congress themes were:- New Methods in Heterocyclic Chemistry- Biologically Active Heterocycles (Pharmaceuticals/Agrochemicals)- Heterocyclic Natural Products and their Analogues- Applications of Heterocycles in Organic Synthesis- Heterocycles in Materials ScienceBesides the collection of 9 papers that are based on the plenary and invited lectures included in this issue of Pure and Applied Chemistry, the ICHC-22 Book of Abstracts is available online and can be downloaded for free from http://www.ichc2009.ca/abstract_book.pdf in pdf format.ICHC-23 will be held in Glasgow, Scotland, 31 July to 5 August 2011 with the following five main themes of heterocyclic chemistry: synthetic methodology, natural products and complex molecule synthesis, materials, medicinal chemistry, and nanochemistry. The conference will be chaired by Prof. Colin Suckling (University of Strathclyde).The organizers are grateful to all who contributed to a successful scientific program, especially to the speakers and to our public and private sponsors: City of St. John's, Memorial University of Newfoundland, IUPAC, Thieme, Wiley-Blackwell, Elsevier, Taiho Pharmaceutical Co., ChemRoutres Corporation, and American Diagnostica, Inc.Paris E. GeorghiouConference Editor

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Kaur, Navjeet. "Photochemical Reactions for the Synthesis of Six-Membered O-Heterocycles." Current Organic Synthesis 15, no. 3 (April 27, 2018): 298–320. http://dx.doi.org/10.2174/1570179414666171011160355.

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Background: The chemists have been interested in light as an energy source to induce chemical reactions since the beginning of the scientific chemistry. This review summarizes the chemistry of photochemical reactions with emphasis of their synthetic applications. The organic photochemical reactions avoid the polluting or toxic reagents and therefore offer perspectives for sustainable processes and green chemistry. In summary, this review article describes the synthesis of a number of six-membered O-heterocycles. Objective: Photochemistry is indeed a great tool synthetic chemists have at their disposal. The formation of byproducts was diminished under photochemical substrate activation that usually occurred without additional reagents. Photochemical irradiation is becoming more interesting day by day because of easy purification of the products as well as green chemistry. Conclusion: This review article represents the high applicability of photochemical reactions for organic synthesis and research activities in organic photochemistry. The synthesis of heterocyclic molecules has been outlined in this review. Traditional approaches require expensive or highly specialized equipment or would be of limited use to the synthetic organic chemist due to their highly inconvenient approaches. Photochemistry can be used to prepare a number of heterocycles selectively, efficiently and in high yield.

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Adak, Laksmikanta, and Tubai Ghosh. "Recent Progress in Iron-Catalyzed Reactions Towards the Synthesis of Bioactive Five- and Six-Membered Heterocycles." Current Organic Chemistry 24, no. 22 (December 18, 2020): 2634–64. http://dx.doi.org/10.2174/1385272824999200714102103.

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Heterocyclic compounds are the largely diverse organic molecules and find prevalent applications in the fine chemical industry, medicinal chemistry and agricultural science. They are also among the most commonly bearing frameworks in numerous drugs and pharmaceutical substances. Therefore, the development of convenient, efficient and environmentally benign methods to produce various types of heterocyclic compounds is an attractive area of research. For the synthesis and functionalization of heterocycles, enormous achievements have been attributed over the past decades. Recently, ironcatalyzed reactions have accomplished a noteworthy development in the synthesis of heterocycles. This review highlights some remarkable achievements in the iron-catalyzed synthesis of heterocyclic compounds published in the last five years.

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Yadav, Shailendra, Sushma Singh, and Chitrasen Gupta. "A CONCISE OVERVIEW ON HETEROCYCLIC COMPOUNDS EXHIBITING PESTICIDAL ACTIVITIES." International Journal of Advanced Research 9, no. 08 (August 31, 2021): 989–1004. http://dx.doi.org/10.21474/ijar01/13352.

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Heterocyclic compounds are numerous and diverse group of organic compounds. Heterocycles are abundantly found in nature and express various physiological properties. Heterocycles are intricately linked to all aspects of life. There are many heterocyclic compounds currently known, and the number is constantly rising owing to extensive synthetic development and their applications. Heterocyclic compounds are used significantly in a number of areas, including biochemistry and medicinal chemistry, and some others. They are predominantly synthesized in agrochemical and pharmaceutical industries due to their potential biological activities. This review article focuses on recently synthesized heterocyclic compounds and their different pesticidal activities such as antifungal, antibacterial, antiviral, nematocidal, insecticidal, acaricidal, and herbicidal.

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Dissertations / Theses on the topic "Heterocyclic chemistry"

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Perrins, Ross. "Heterocyclic chemistry of trithiazyl trichloride." Thesis, Imperial College London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283411.

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Jones, Louise. "Combinatorial, heterocyclic and guanidine chemistry." Thesis, Bangor University, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429865.

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Henderson, Neil. "Studies in nitrogen heterocyclic chemistry." Thesis, University of East Anglia, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.280300.

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Simcox, Michael Thomas. "Some aspects of nitrogen heterocyclic chemistry." Thesis, Loughborough University, 1997. https://dspace.lboro.ac.uk/2134/10544.

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Chapter One reviews the use of scandium and lanthanide trifluoromethanesulfonates (triflates) in organic synthesis. Their ability to act as Lewis acids and so promote a wide variety of reactions are illustrated. In particular the review highlights the advantages of scandium and lanthanide triflates over more conventional Lewis acids, such as aluminium(I1I) chloride. Chapter Two describes the use of scandium and lanthanide trifiates in the reaction of acetals with amines to produce imines. The extension of this methodology to the synthesis of nitrogen-containing heterocycles such as isoindolones, isoquinolinones and ~-carboline derivatives are elaborated on. Some limitations of the methodology and the problems encountered with its application to the synthesis of enamines are covered. Chapter Three reports our approach to a novel synthesis of ~-carboline derivatives. The formylation of indole-3-acetic acid derivatives in the 2- position proved difficult and several approaches to this problem are discussed. The attempted cyclisation of imines prepared from 2-formyl- and 2- acetyl-3-indolyl acetic acid compounds are also covered. Chapter Four describes a modified Clauson-Kaas pyrrole procedure using trimethylsilyl trifiate. The selection of reaction conditions in an effort to optimise the procedure are discussed. Chapter Five provides full experimental procedures and analytical data for the reactions described in Chapters Two, Three and Four.

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Civcir, Pervin Unal. "Extended heterocyclic systems." Thesis, University of East Anglia, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.332359.

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Karatza, Mary-Helen. "Extended heterocyclic systems." Thesis, University of East Anglia, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359850.

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Collier, Steven James. "Heterocyclic ortho-quinodimethanes." Thesis, University of Liverpool, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366249.

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White, Lindsay Anne. "Heterocyclic o-quinodimethanes." Thesis, University of Liverpool, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.262608.

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Lapinsky, David J. "STUDIES IN AZIRIDINE-ALLYLSILANE CHEMISTRY: EXTENSION OF SCOPE." Columbus, OH : Ohio State University, 2002. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1038954949.

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Thesis (Ph. D.)--Ohio State University, 2003.
Title from first page of PDF file. Document formatted into pages; contains xx, 256 p.: ill. (some col.). Includes abstract and vita. Advisor: Stephen C. Bergmeier, College of Pharmacy. Includes bibliographical references (p. 234-256).

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Pedersen, Jan Mondrup. "Amides as radical precursors in heterocyclic chemistry." Thesis, Loughborough University, 2005. https://dspace.lboro.ac.uk/2134/34502.

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In this project the use of amides as precursors for imidoyl radicals in heterocyclic chemistry has been developed. Amides were converted to thioamides, which function as precursors for imidoyl radical equivalents. Also, a novel protocol for the synthesis of imidoyl selanides was developed for the purpose of using these as imidoyl radical precursors. The precursors were used in a study of intramolecular oxidative cyclisation of imidoyl radicals onto electron deficient pyrroles and indoles. The imidoyl radical equivalents derived from thioamides did not cyclise onto heteroarene double bonds. In contrast, imidoyl radicals derived from imidoyl selanides did cyclise 6-exo onto activated heteroarenes, but yields were generally low due mainly to competing reduction of the imidoyl radical, but also due to adduct formation with isobutyronitrile radicals originating from the initiator.

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Books on the topic "Heterocyclic chemistry"

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Abel, E. W., ed. Heterocyclic Chemistry. Cambridge: Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847551061.

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Suschitzky, H., and O. Meth-Cohn, eds. Heterocyclic Chemistry. Cambridge: Royal Society of Chemistry, 1985. http://dx.doi.org/10.1039/9781847556325.

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Suschitzky, H., ed. Heterocyclic Chemistry. Cambridge: Royal Society of Chemistry, 1986. http://dx.doi.org/10.1039/9781847556332.

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Gupta, Radha Raman, Mahendra Kumar, and Vandana Gupta. Heterocyclic Chemistry. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-662-07757-3.

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Gupta, Radha Raman, Mahendra Kumar, and Vandana Gupta. Heterocyclic Chemistry. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-72276-9.

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Joule, J. A., K. Mills, and G. F. Smith. Heterocyclic Chemistry. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8.

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Gilchrist, T. L. Heterocyclic chemistry. Harlow, Essex, Eng: Longman Scientific & Technical, 1989.

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(Keith), Mills K., and Knovel (Firm), eds. Heterocyclic chemistry. 4th ed. Malden, MA: Blackwell Science, 2000.

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Royal Society of Chemistry (Great Britain), ed. Heterocyclic chemistry. Cambridge, UK: Royal Society of Chemistry, 2001.

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Joule, J. A. Heterocyclic chemistry. 5th ed. Hoboken, N.J: Wiley, 2009.

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Book chapters on the topic "Heterocyclic chemistry"

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Gupta, Radha Raman, Mahendra Kumar, and Vandana Gupta. "Heterocyclic Synthesis." In Heterocyclic Chemistry, 159–273. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-72276-9_5.

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Gupta, Radha Raman, Mahendra Kumar, and Vandana Gupta. "Aromatic Heterocycles." In Heterocyclic Chemistry, 39–104. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-72276-9_3.

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Gupta, Radha Raman, Mahendra Kumar, and Vandana Gupta. "Nonaromatic Heterocycles." In Heterocyclic Chemistry, 105–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-72276-9_4.

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Joule, J. A., K. Mills, and G. F. Smith. "Structures and main physical properties of aromatic heterocycles." In Heterocyclic Chemistry, 1–17. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_1.

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Joule, J. A., K. Mills, and G. F. Smith. "Typical reactivity of the diazines: pyridazine, pyrimidine and pyrazine." In Heterocyclic Chemistry, 185–88. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_10.

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Joule, J. A., K. Mills, and G. F. Smith. "The diazines: pyridazine, pyrimidine and pyrazine: reactions and synthesis." In Heterocyclic Chemistry, 189–224. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_11.

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Joule, J. A., K. Mills, and G. F. Smith. "Typical reactivity of pyrroles, thiophenes and furans." In Heterocyclic Chemistry, 225–28. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_12.

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Joule, J. A., K. Mills, and G. F. Smith. "Pyrroles: reactions and synthesis." In Heterocyclic Chemistry, 229–58. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_13.

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Joule, J. A., K. Mills, and G. F. Smith. "Thiophenes: reactions and synthesis." In Heterocyclic Chemistry, 259–77. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_14.

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Joule, J. A., K. Mills, and G. F. Smith. "Furans: reactions and synthesis." In Heterocyclic Chemistry, 278–300. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_15.

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Conference papers on the topic "Heterocyclic chemistry"

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Šíbor, Jiří, and Aleš Bárta. "NEW WAYS OF HETEROCYCLIC CHEMISTRY TEACHING." In 12th International Technology, Education and Development Conference. IATED, 2018. http://dx.doi.org/10.21125/inted.2018.1210.

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Torroba, Tomas, Oleg Rakitin, and Charles Rees. "New heterocyclic materials." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01781.

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Mangalagiu, Violeta, Dumitrela Diaconu, Costel Moldoveanu, Gheorghita Zbancioc, Ramona Danac, Dorina Amariucai-Mantu, Vasilichia Antoci, and Ionel Mangalagiu. "Hybrid and chimeric nitrogen heterocycles with biological activity." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab01.

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Nitrogen heterocycles, especially azine and azole derivatives, are highly valuable scaffolds in medicinal chemistry, being the core components of a large variety of drugs with variously biological activity such as antiplasmodial and antimalarial, antitubercular, antibacterial, antifungal, anticancer, analgesic, antidepressant, anxiolytics, antihypertensive, anticoagulants, diuretics, etc. As a result, obtaining of such entities continues to arouse a strong interest from academia and industry. As part of our ongoing research in the area of nitrogen heterocyclic derivatives, we present herein some representative results obtained by our group in the field of hybrid and chimeric azahetrocycles compounds with antimicrobial and anticancer activity. Chemistry, anticancer, antibacterial, antifungal and antituberculosis activity of compounds is presented. Some of the hybrid and chimeric structures possess a good anticancer and/or antimicrobial activity.

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Shutalev, Anatoly. "New Synthetic Application of Ureidoalkylation in Heterocyclic Chemistry." In The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02013.

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Stanovnik, Branko. "3-Dimethylaminopropenoates and Related Compounds in the Synthesis of Heterocyclic Systems and Heterocyclic Amino Acids." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01783.

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Schnell, Barbara, and Thomas Kappe. "Sulfidation of Heterocyclic 1,3-Dicarbonyl Systems ." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01720.

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Resende, Diana, Emília Sousa, Mariana Almeida, Bruna Maciel, Helena Carmo, Isabel Almeida, José Sousa Lobo, et al. "New heterocyclic polyphenols with skin anti-aging potential." In 5th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06362.

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Biliavska, Liubov, Yulia Pankivska, Olga Povnitsa, Svitlana Zagorodnya, Ganna Gudz, Nadiia Pikun, and Yuriy Shermolovich. "Antiviral Activity of Fluorinated Heterocyclic Compounds." In 2nd International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecmc-2-a019.

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Maiboroda, D. A., V. V. Scherbukhin, and E. V. Babaev. "Computer design of heterocyclic ring-opening reactions." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47787.

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Ha, Sie-Tiong, Guan-Yeow Yeap, Teck-Leong Lee, and Teck-Ming Koh. "New Heterocyclic Liquid Crystals with Benzothiazole Core." In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00373.

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