The 23rd International Electronic Conference on Synthetic Organic Chemistry
Part of the Electronic Conference on Synthetic Organic Chemistry series
15 Nov–15 Dec 2019
General Organic Synthesis, Bioorganic, Medicinal and Natural Products Chemistry, Microwave Assisted Synthesis, Polymer and Supramolecular Chemistry, Computational Chemistry, Ionic Liquids
- Go to the Sessions
- Event Details
Welcome from the Chair
Welcome to the 23rd International Electronic Conference on Synthetic Organic Chemistry
Electronic conferences on synthetic organic chemistry (ECSOC) are a series of conferences maintained through the internet since 1997, an original initiative by MDPI, and later consolidated with the contribution of the University of Santiago de Compostela (Spain). Nowadays it constitutes the first and oldest electronic conference in the world. It maintains its character of free participation, with contributions considered as preliminary reports on edge achievements, and registration as a distinctive standard of the world wide web open access character.
It covers different sections of organic synthesis:
- General Organic Synthesis
- Bioorganic, Medicinal and Natural Products Chemistry
- Microwave Assisted Synthesis
- Polymer and Supramolecular Chemistry
- Computational Chemistry
- Ionic Liquids
Call for Papers
Dear Colleague,
The Electronic Conferences on Synthetic Organic Chemistry (ECSOC) are a series of conferences that have been held online since 1997. Originally, it was an initiative of MDPI, and was later amalgamated with the University of Santiago de Compostela (Spain). It now constitutes the longest running electronic conference in the world. It maintains free participation and registration in the true spirit of open access on the World Wide Web. The conference this year will cover a wide range of aspects involved in synthetic organic chemistry. A non-exhaustive list of topics that will be considered comprises:
- General Organic Synthesis
- Bioorganic, Medicinal and Natural Products Chemistry
- Microwave Assisted Synthesis
- Polymer and Supramolecular Chemistry
- Computational Chemistry
- Ionic Liquids
ECSOC-23 offers you the opportunity to participate in this international, scholarly conference without having the concern or expenditure of travel. The conference will be completely free of charge—both to “attend”, and for scholars to upload and present their latest work on the conference platform. There will be a possibility to submit selected papers to the journal Molecules (ISSN 1420-3049, Impact Factor: 3.098 (2017) ; 5-Year Impact Factor: 3.268 (2017); https://www.mdpi.com/journal/molecules).
Abstracts (in English) should be submitted by *30 October 2019* online at https://sciforum.net/conference/ecsoc-23. After the abstract is accepted by the Scientific Committee, the authors will be invited to prepare a full description of their work under the form of a PowerPoint presentation, and to upload it *before 15 November 2019* to ensure there is time for a final check.
We hope you will be able to join this exciting event and support us in making it a success. The 23rd International Electronic Conference on Synthetic Organic Chemistry is organized and sponsored by MDPI (https://www.mdpi.com), an open access publisher based in Switzerland.
We look forward to receiving your research papers and to welcome you at this 23rd edition of the e-Conference.
Please do not hesitate to contact us if you have questions.
Kind regards,
*Dr. Julio A. Seijas Vázquez*
Chair of the 23rd Electronic Conference on Synthetic Organic Chemistry (ECSOC 23)
Instructions for Authors
Submissions should be done by the authors online by registering with www.sciforum.net, and using the "New Submission" function once logged into system.
- Scholars interested in participating with the conference can submit their abstract (about 200-250 words covering the areas of manuscripts for the proceedings issue) online on this website until 25 October 2019.
- The Conference Committee will pre-evaluate, based on the submitted abstract, whether a contribution from the authors of the abstract will be welcome for the 23rd International Electronic Conference on Synthetic Organic Chemistry. All authors will be notified by 1 November 2019 about the acceptance of their abstract.
- If the abstract is accepted for this conference, the author is asked to submit the manuscript, optionally along with a PowerPoint and/or video presentation of his/her paper (only PDF), until the submission deadline of 17 November 2019.
- The conference proceedings papers and presentations will be available on https://sciforum.net/conference/ecsoc-23 for discussion and will be published in Journal Proceedings.
- Participants of this conference are cordially invited to contribute with a full manuscript to our Special Issue in the journal Molecules (the submission to the journal is independent from the conference proceedings and will follow the usual process of the journal, including peer-review, APC, etc.). Papers presented at the conference will be granted a 20% discount in the Special Issue.
First page:
Title
Full author names
Affiliations (including full postal address) and authors' e-mail addresses
Abstract (200-250 words)
Keywords
Introduction
Methods
Results and Discussion
Conclusions
(Acknowledgements)
References
Authors are encouraged to prepare a presentation in PowerPoint or similar software, to be displayed online along with the Manuscript. Slides, if available, will be displayed directly in the website using Sciforum.net's proprietary slides viewer. Slides can be prepared in exactly the same way as for any traditional conference where research results can be presented. Slides should be converted to the PDF format before submission so that our process can easily and automatically convert them for online displaying.
.MPEG4
.MP4
.AVI
.WMV
.MPEGPS
.FLV
Figures, Schemes and Tables: Authors are encouraged to prepare figures and schemes in color. Full color graphics will be published free of charge. Figure and schemes must be numbered (Figure 1, Scheme I, Figure 2, Scheme II, etc.) and a explanatory title must be added. Tables should be inserted into the main text, and numbers and titles for all tables supplied. All table columns should have an explanatory heading. Please supply legends for all figures, schemes and tables. The legends should be prepared as a separate paragraph of the main text and placed in the main text before a table, a figure or a scheme.
List of accepted submissions (124)
Id | Title | Authors | Presentation Video | Poster PDF | |||||||||||||||||||||||||||||||||||||
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sciforum-026715 | Morphological and chemical analysis of the molecularly-imprinted polymer-based D-arabinose sensor on a modified electrode with functionalized carbon nanotubes | , , , | N/A | N/A |
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The development of renewable fuels is driven by different countries due to future shortages of fossil fuels and damage to the environment caused by their use. A promising alternative to replace the growing energy crisis and reduce environmental damage is second generation ethanol, which can be produced from sugarcane-based lignocellulosic biomass, an excellent raw material with high availability and abundance that does not cause competition with energy sources. Second generation production, generally characterized by preprocessing, hydrolysis and fermentation, is not as advanced as first generation production. However, with continuous scientific effort, this change can be altered. A clear understanding of the chemical changes that occur through hydrolysis of lignocellulosic biomass is critical to process control and optimization. In this sense, the development of graphite and paraffin composite sensors, modified with carbon nanotubes (FMWCNTs) and molecularly printed polymers (MIPs) for the determination of D-arabinose is an excellent option, because these sensors have high selectivity and sensitivity in the analyzes.For this reason, the present work presents a chemical study of the functional groups of the chemical species present on the surfaces of the materials using the Fourier Transform Infrared Spectroscopy (FTIR) technique and a morphological analysis by the Scanning Electron Microscopy (SEM) technique. |
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sciforum-026730 | Anthracene-Oxazine based reversible ink | , | N/A | N/A |
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Anthracene fluorophore and an oxazine chromophore get coupled within the same molecular configuration to produce a molecular machine based receptor 1. On treatment with TFA, the oxazine closed form gets open in conjugation with the 1, 3, 3-Trimethylindoline species. This molecular change produces a bathochromic shift of 140nm directly from UV to Visible region in association with intense pink color. This molecule can be used as molecular ink to print a different colored decoration on paper. Upon addition with TEA, the colored open forms of the receptor revert to its original colorless form to rub the printed impression. Thus, the simple paper can be used for multiple times to achieve the write-read-erase strategy. This photoswitchable molecular motif can evolve many opportunities in the industry for printing purpose and huge paper consumption. |
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sciforum-027127 | Synthesis and characterization of new biocompatible amino amphiphilic compounds derived from oleic acid as nanovectors for drug delivery | , , | N/A | N/A |
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Amphiphilic molecules have been actively explored as promising materials in the field of bio and nanotechnology. These molecules are constituted by a polar head and a lipophilic tail and in an aqueous medium are self-assemble to form different types of macromolecular structures such as micelles, monolayer vesicles, bars, sheets and tubes. In this work, a convergent synthetic approach for the synthesis of two new amphiphilic compounds based on a versatile amino polar head, a tetraethylene glycol spacer and a lipophilic tail derived from oleic acid has been developed. Subsequently, after a self-assembly process in aqueous medium, nanostructures as micelles have been obtained and characterized. Finally, a procedure for the inclusion of the highly lipophilic drug Dexamethasone has been carried out in order to study the ability of these micelles to act as nanovectors for drug delivery. |
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sciforum-027329 | ZnBr2 functionalized ionic liquid: An efficient solvent and catalyst for the facile synthesis of 1-benzamino-1,4-dihydropyridine | , , | N/A | N/A |
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Ionic liquids (ILs) are mostly composed of organic cations and organic/inorganic anions. One of the most important classes of ILs are imidazolium ILs. [1]. The hydrophilicity and hydrophobicity of ILs are regbenzohydrazidularly influenced by the length of alkyl side chain of cation. According to this effect, better hydrophilicity comes from a shorter alkyl side chain and on the contrary, better hydrophobicity comes from a lengthier alkyl side chain of cation. Typical ILs have exceptional properties. Most ILs are stable at about 300 oC in the liquid state at normal conditions. Due to the exceptional properties of ILs, they have been used in diverse industries including batteries and fuels. As solvents, ILs have been employed in many chemical fields. Solubilities of ILs with organic/inorganic species are completely satisfactory. Here, by N-methyl imidazole (Im), 1,3-dibromopropane, triethanolamine (TEA), and ZnBr2, new ionic liquid (TEA-Im-Zn) was synthesized and used as catalyst and solvent in the synthesis of functionalized 1-benzamino-1,4-dihydropyridine using aromatic aldehyde, malononitrile, triethylamine, arylamine and dialkyl acetylenedicarboxylate. |
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sciforum-027338 | Use of PPh3-BrCCl3 in the preparation of acylhydrazines, N-methylamides, anilides and N-arylmaleimides from carboxylic acids | , , , | N/A | N/A |
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In certain countries, many of the reagents used to transform carboxylic acids to acyl halides such as phosphorus trichloride, phosphorus tribromide, phosphorus pentachloride, phosphoryl chloride, thionyl chloride and sulfuryl chloride are difficult to come by. Against this background, the authors developed the reaction system triphenylphosphine (PPh3) – bromotrichloromethane (BrCCl3) to prepare acyl halides in situ. In the following, the use of this reagent combination is joined with the reaction of the in situ prepared acyl halides with nitrogen nucleophiles, specifically with hydrazines, methylamine and anilines. The reaction is also used in an intramolecular variant by the reaction of maleanilic acids to N-arylmaleimides. |
Conference Committee
Name |
Role |
Affiliation |
Dr. Julio A. Seijas |
Conference Chair |
Universidad de Santiago de Compostela |
Dr. M. Pilar Vázquez-Tato |
Conference Sci. Secretary |
Universidad de Santiago de Compostela |
Committee Member |
Universidade de Santiago de Compostela. Spain |
|
Committee Member |
Université Aboubakr Belkaid. Algeria |
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Committee Member |
Iran University of Science & Technology. Iran |
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Committee Member |
Oakland University. USA. |
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Committee Member |
Institute of Chemistry Timisoara of Romanian Academy. Romania |
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Committee Member |
Universidade Federal do Rio de Janeiro. Brazil |
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Committee Member |
Università degli Studi di Perugia. Italy |
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Committee Member |
Universidad de Guanajuato. México |
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Committee Member |
Technische Universität Dresden. Germany |
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Committee Member |
Birla Institute of Technology. India |
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Committee Member |
Instituto de Química Orgánica General CSIC. Spain |
|
Committee Chair |
. Faculty of Pharmacy, Comenius University in Bratislava, Slovakia |
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Committee Member |
Wilson College, University of Mumbai. India |
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Committee Member |
Universidade de Santiago de Compostela. Spain |
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Committee Member |
Masaryk University. Czech Republic |
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Committee Member |
Universidade do Minho. Portugal |
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Committee Member |
University of Perugia. Italy |
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Committee Member |
Real Sociedad Española de Química (RSEQ). Spain |
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Committee Member |
Russian Academy of Sciences. Russian Federation |
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Committee Member |
University of Costa Rica. Costa Rica |
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Committee Member |
Karl-Franzens Universität .Austria |
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Committee Member |
Université de La Rochelle. France |
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Committee Member |
Universidad de Vigo. Spain |
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Committee Member |
United Arab Emirates University. United Arab Emirates |
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Committee Member |
Universidade de Santiago de Compostela. Spain |
Conference Secretaries
Dr. M. Pilar Vázquez-Tato. Universidade de Santiago de Compostela. Spain
pilar.vazquez.tato@usc.es
Ms. Judith Wu
ecsoc@mdpi.com