Welcome from the Chairs

Name: The 3rd International Electronic Conference on Synthetic Organic Chemistry
Start: 1999-10-31T23:00:00
End: 1999-11-29T23:00:00

Welcome to The 3rd International Electronic Conference on Synthetic Organic Chemistry

Call for Papers

This will be the 3rd meeting of ECSOC. All accepted presentations will be posted on this website during the conference. Discussions will be possible by using online commenting and reply functions. The Proceedings will be published later online and as a CD-ROM edition. Posters presented may be considered as preliminary communications of new research results or review papers and may be published in another form later in any standard journal. At the authors discretion, contributions will be removed from the web-site after the end of the conference and not included in the online and CD-ROM proceedings editions. Authors are invited to publish their papers subsequently in Molecules.

Sessions

A. General Organic Synthesis
B. Combinatorial Synthesis, Parallel Synthesis and Automation
C. Medicinal and Bioorganic Application of Organic Synthesis
D. Natural Product Isolation and Modification
E. Information and Compound Archives Management and Internet Application

Instructions for Authors

Proceedings Paper

Communications for the proceedings issue must have the following organization:

Firstpage:

Title

Full author names

Affiliations and authors' e-mail addresses

Abstract

Keywords

Introduction

Results and Discussion

Experimental Procedure

(Acknowledgements)

References

Communications should be prepared in MS Word. The publication format will be PDF.

Presentation Slides
Authors are encouraged to preare a couple of slides in PowerPoint or similar software, to be displayed online along with the Communication. 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 PDF format before submission.

Submission
Submissions should be done by the authors online by registering with www.sciforum.net, and using the "new submission" function once logged into system.

Copyright
MDPI AG, the publisher of the Sciforum.net platform, is an open access publisher. We believe that authors should retain the copyright to their scholarly works. Hence, by submitting a Communication paper to this conference, you retain the copyright of your paper, but you grant MDPI AG the non-exclusive right to publish this paper online on the Sciforum.net platform. This means you can easily submit your paper to any scientific journal at a later stage and transfer the copyright to its publisher (if required by that publisher).

List of accepted submissions (68)

Id	Title	Authors	Poster PDF
sciforum-000767	Cyclizations of 5,6-difunctionalized pyrido[2,3-d]pyrimidinetriones Wolfgang Stadlbauer , Dang Van Tinh Submitted: 31 Oct 1999 Abstract: Show Abstract	Wolfgang Stadlbauer , Dang Van Tinh	N/A	Show Abstract
Pyrido[2,3-d]pyrimidine systems A are of chemical and chemotherapeutical interest because they show both the properties of a 4-hydroxy-2-pyridone (present in a series of natural products and biologically active structures, e.g. [1]) and of uracil in one ring system.
sciforum-000768	Influence of Some Thia or Azasubstituted Butyric Acid Derivatives on Chemical Shift of Carbon Atom of Benzene Ring. Johannes Fröhlich , Fritz Sauter , Viktor Milata Submitted: 31 Oct 1999 Abstract: Show Abstract	Johannes Fröhlich , Fritz Sauter , Viktor Milata	N/A	Show Abstract
Eight thia- or azasubstituted butyric acid derivatives was prepared and influence of this substituent onto carbon atoms of benzene ring was studied
sciforum-000769	Stereoselective a-Oxyfunctionalisation of Benzo(hetera)cyclanones by Dimethyldioxirane. Attila Kiss , Joszsef Jeko , Albert Lévai , Tamos Patonay Submitted: 31 Oct 1999 Abstract: Show Abstract	Attila Kiss , Joszsef Jeko , Albert Lévai , Tamos Patonay	N/A	Show Abstract
a-Hydroxy ketones including their cyclic derivatives are important synthetic building blocks. Chiral, non-racemic a-hydroxy ketones (and esters) are widespread in natural products. Therefore, there is a high demand to develop efficient methods for the construction of their enantiopure or at least enantiomerically enriched representatives and a number of procedures have been published in the last decades [1,2]. Our interest in the synthesis of a-hydroxy benzo(hetera)cyclanones, particularly 3-hydroxychromanones, prompted us to investigate the synthetic utility of the recently developed electrophilic chiral oxidizing system, namely dimethyldioxirane (DMD)/Jacobsen's catalyst [3] in the oxyfunctionalization of enol derivatives. Enol acetates were choosen as prochiral substrates because their higher stability as compared to silyl enol ethers and their high reactivity toward DMD
sciforum-000770	Indole, Cinnoline, Benzothiazine and Dihydrofuroquinoline Derivatives from Aryldifurylmethanes. Alexander Butin , Vladimir Abaev , Tat'yana Stroganova , Andrey Gutnov , Irina Lodina , Olga Shurakova Submitted: 31 Oct 1999 Abstract: Show Abstract	Alexander Butin , Vladimir Abaev , Tat'yana Stroganova , Andrey Gutnov , Irina Lodina , Olga Shurakova	N/A	Show Abstract
Until recently the most publications on furylarylmethanes were devoted to their application as promising source for polymer producing [1-3] or as intermediates in the synthesis of calixarenes and crown ethers [4, 5]. At the same time, due to the availability of furan ring in the molecules of these compounds they can serve as convenient and useful precursors for syntheses of various heterocyclic compounds condensed with benzene cycle. But looking through the literature we could find only one example of similar use of furylarylmethanes: Prof. Gurnos Jones and co-workers obtained carbazole derivative from 2-nitrophenyldifurylmethane under treatment of latter with triethylphosphite
sciforum-000771	Symmetric Difuryl- and Trifurylmethanes: General Methods of Synthesis Tat'yana Stroganova , Alexander Butin , Lyudmila Sorotskaya , Vladimir Kul'nevich Submitted: 31 Oct 1999 Abstract: Show Abstract	Tat'yana Stroganova , Alexander Butin , Lyudmila Sorotskaya , Vladimir Kul'nevich	N/A	Show Abstract
Although at last time the most of investigators put their attention to development of convenient approaches to synthesis of asymmetric furylhetarylalkanes, symmetric di- and trifurylmethanes keep their importance as before. Some derivatives of difurylalkanes use in various fields of industry. Our stydies let us to elaborate convenient routes to several derivatives of symmetric di- and trifurylmethanes series.