The 19th International Electronic Conference on Synthetic Organic Chemistry

Name: The 19th International Electronic Conference on Synthetic Organic Chemistry
Start: 2015-10-31T23:00:00
End: 2015-11-29T23:00:00

Part of the Electronic Conference on Synthetic Organic Chemistry series

Welcome from the Chairs

Welcome to the 19th 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:

A. General Organic Synthesis

B. Bioorganic, Medicinal and Natural Products Chemistry

C. Microwave Assisted Synthesis

D. Polymer and Supramolecular Chemistry

E. Computational Chemistry

F. Ionic Liquids

Conference Chairs

Julio A. Seijas

Universidad de Santiago de Compostela

Lucy Lu

MDPI AG

Sessions

A. General Organic Synthesis
B. Bioorganic, Medicinal and Natural Products Chemistry
C. Microwave Assisted Synthesis
D. Polymer and Supramolecular Chemistry
E. Computational Chemistry
F. Ionic Liquids

List of accepted submissions (103)

Id	Title	Authors	Poster PDF
sciforum-006035	A simple, convenient three component one-pot procedure for the synthesis of benzimidazolo-quinazolinone derivatives in the presence Silica-based sulfonic acid (MCM-41-SO3H): a efficient and practical catalyst Mohammad Reza Naimi-Jamal , Maryam Karimi Submitted: 07 Sep 2015 Abstract: Show Abstract	Mohammad Reza Naimi-Jamal , Maryam Karimi	N/A	Show Abstract
A variety of quinazolinones are readily prepared via one-pot three-component reaction in good to excellent yields. The desired products were obtained from the reaction of dimedone, various aldehydes with 2-aminobenzimidazole under mild reaction conditions using MCM- 41-SO3H as effective catalyst in green and reusable catalyst in refluxing ethanol has been developed. Starting from the corresponding available materials, this friendly and environmentally free-metal procedure has been successfully extended to the synthesis of benzimidazoquinazolinones. The salient advantages of this method are mild reaction conditions, nontoxic and inexpensive catalyst, environmentally benign, high to excellent yields, shorter reaction times, easy operation, and no column chromatographic separation.[1,2] [1] M. Heravi, F. Derikvand, L. Ranjbar, “Sulfamic acid–catalyzed, threeComponent, one-pot synthesis of [1, 2, 4] triazolo/benzimidazolo quinazolinone derivatives”, synthetic communications, 2010, 677–685. [2] Gh. H. Mahdavinia, M. M. Ghanbari, H. Sepehrian, F. Kooti, “MCM-41 functionalized sulfonic acid catalyzed one-pot synthesis of 1,8-dioxo-octahydroxanthenes”, 2010, 117-120.
sciforum-006617	Highlight on the reactivity of PhSeZnX Bonifacio Monti , Luca Sancineto , Martina Palomba , Luana Bagnoli , Francesca Marini , Eder Lenardao , Claudio Santi Submitted: 23 Oct 2015 Abstract: Show Abstract	Bonifacio Monti , Luca Sancineto , Martina Palomba , Luana Bagnoli , Francesca Marini , Eder Lenardao , Claudio Santi	N/A	Show Abstract
The first bench stable selenolates, PhSeZnHalides have been synthesized through a completely atom economy oxidative insertion of the elemental zinc on the commercially available PhSeHalides. These reagents showed the characteristic nucleophilic reactivity which will be reviewed in this report. All of the reactions were strongly accelerated when effected in water suspension. Alkyl, aryl, vinyl and acyl substitutions, ring-opening reactions of epoxides and aziridines and Michael type addition will be described including the role of the zinc in the control of the chemoselectivity and stereoselectivity.
sciforum-006569	Superbasic system CsOH/DMSO as a reagent for a fast one-step synthesis of symmetrical dialkyl trithiocarbonates ali yousefi Submitted: 17 Oct 2015 Abstract: Show Abstract	ali yousefi	N/A	Show Abstract
Symmetrical dialkyl trithiocarbonates were readily synthesized in excellent yields by one-step reaction of carbon disulfide and various alkyl halides under mild reaction conditions in the presence of cesium hydroxide as a super basic system. This method provides a synthesis of symmetrical dialkyl trithiocarbonates in short reaction times without the use of highly toxic starting materials.
sciforum-005985	A new synthesis of cellulose-based silver nanocomposite and its catalytic performance Ali Maleki , Hamed Movahed , Reza Paydar Submitted: 24 Aug 2015 Abstract: Show Abstract	Ali Maleki , Hamed Movahed , Reza Paydar	N/A	Show Abstract
In the present work, cellulose-based silver nanocomposite is synthesized by a new method and used as a catalyst for the synthesis of heterocyclic compounds. To study the morphology and characterization of the nanocomposite, scanning electron microscopy (SEM) and X-ray diffraction (XRD) were obtained.
sciforum-006527	*An efficient synthesis of bis(indolyl) methanes and N, N'-alkylidene bisamides by silzic under solvent free conditions* Hanan Soliman , Ahmed Mubarak , Saad Elmorsy Submitted: 14 Oct 2015 Abstract: Show Abstract	Hanan Soliman , Ahmed Mubarak , Saad Elmorsy	N/A	Show Abstract
An operationally simple and green method for the synthesis of a wide range of bis(indolyl)methanes, and N,N'-alkylidene bisamides under mild conditions, with excellent yields using silzic, has been developed. This improved method furnishes in good yields bis(indolyl)methanes derivatives starting from indole and aldehydes, or ketones, and N,N'-alkylidene bisamides derivatives starting from acetamide and aldehydes. the catalytic system was reused up for three times with The same efficiency