Welcome from the Chairs

Welcome to The 11th International Electronic Conference on Synthetic Organic Chemistry

Call for Papers

The research concerned with synthetic organic chemistry is progressing fast and simultaneously, activities within both industry and academy are becoming more globalized. Successful research requires interaction with several units around the world. We are facing an obvious need for new and fast types of communication within our scientific community. Sciforum.net electronic conferences provide a platform for fast exchange of the latest research findings, as well as a possibility for global meetings with no limitations related to traveling.

The 11th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-11) will run from 1 - 30 November 2007. ECSOC-11 Proceedings will be published later online and as a CD-ROM edition. Posters presented at ECSOC-11 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. Solid Phase Chemistry and Combinatorial Synthesis
C. Bioorganic Chemistry and Natural Products
D. Symposium on Selenium and Tellurium Chemistry
E. Symposium on Microwave Assisted Synthesis
F. Supramolecular Chemistry
G. Computational Chemistry

Instructions for Authors

Procedure for Submission, Peer-Review, Revision and Acceptance of Conference Proceedings Papers

Scholars interested in participating with the conference can submit their abstract (about 200-300 words covering the areas of Communications for the proceedings issue) online on this website until 30 September 2007.
The conference committee will pre-evaluate, based on the submitted abstract, whether a contribution from the authors of the abstract will be welcome for this 11th edition of ECSOC. All authors will be notified by 10 October 2007 about the acceptance of their abstract.
If the abstract is accepted for this conference, the author is asked to submit his full communication paper, optionally along with a PowerPoint presentation of his/her paper, until the submission deadline of 20 October 2007.
The conference committee will then organize a round of peer-review of the submitted communication papers, and authors are eventually asked to revise their paper based on peer-reviewer's comments.
Finally, accepted communication papers will appear on the website immediately after their acceptance.
Presented communications papers can be discussed, commented and rated during the time of the conference, 1-30 November 2007.

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
Methods / Experim
Results and Discussion
Conclusions
(Acknowledgements)
References

Communications should be prepared in MS Word or any other word processor and should be converted to the PDF format before submission. The publication format will be PDF. The Communication paper should count at least 3 pages (incl. figures, tables and references). There is no page limit on the length, although authors are asked to keep their papers as concise as possible.

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, 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.

Submission

Submissions should be done by the authors online by registering with www.sciforum.net, and using the "Start 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 (75)

Id	Title	Authors	Poster PDF
sciforum-000407	Synthesis of New 1-Substituted-4-(2-phenylquinazolin-4-yl and 4-ylidene) Walid Fathalla , Pavel Pazdera Submitted: 29 Nov 2007 Abstract: Show Abstract	Walid Fathalla , Pavel Pazdera	N/A	Show Abstract
Two new 1-substituted-4-(2-phenylquinazolin-4-yl and 4-ylidene) thiosemicarbazides 3 and 5 were formed by multistep domino reaction of imidoyl isothiocyanate derivative 1 with 1,1-di-R hydrazine in acetone solution. Applied hydrazine hydrate under the same reaction condition afforded 4-(2-phenylquinazolin-4(3H)-ylidene)-2-(prop-1-en-2-yl)-1- (propan-2-lidene) thiosemicarbazide (7) via six step three component domino reaction. Compounds 3, 5 and 7 were identified by CHNS elemental analysis, 1 H-NMR,13 C-NMR spectral data and their correlation with ones from known structural motives.
sciforum-000408	Convenient Synthesis of Novel Amino Acid Coupled Benzanilides S. El Rayes , Ibrahim Ali , Walid Fathalla Submitted: 29 Nov 2007 Abstract: Show Abstract	S. El Rayes , Ibrahim Ali , Walid Fathalla	N/A	Show Abstract
A facile and convenient synthesis of a variety of Methyl 2-(2-Benzoylaminobenzoylamino) alkanoate 4a-d has been developed by the DCC coupling of 2- Benzoylamino-benzoic acid with amino acid methyl ester. Compounds 4a-c were alternatively prepared by the reaction of aminoacid ester with 3,1-benzoxazinone 2 in pyridine. Dipeptides 8a-j were subsequently prepared following the azide coupling method. Compounds 4 and 8 were expected to possess antimicrobial activity.
sciforum-000412	Quantitative Regeneration of Carbonyl Compounds from Oximes and hydrazones by Gaseous Nitrogen Dioxide H. Hamzehali , M. Naimi-Jamal , J. Mokhtari Submitted: 29 Nov 2007 Abstract: Show Abstract	H. Hamzehali , M. Naimi-Jamal , J. Mokhtari	N/A	Show Abstract
Treatment of various oximes and phenylhydrazones with gaseous nitrogen dioxide at room temperature afforded the corresponding carbonyl compounds in high to quantitative yields and a simple and solventless method.
sciforum-000413	Different Behaviouof of Disubtituted Aromatic Heterocycles in Polar Diels-Alder Reactions Claudia Rosa , Pedro Mancini , Maria Kneeteman Submitted: 29 Nov 2007 Abstract: Show Abstract	Claudia Rosa , Pedro Mancini , Maria Kneeteman	N/A	Show Abstract
Dienophilic behaviour of disubstituted aromatic heterocycles towards normal electron demand Diels-Alder reactions is studied under thermal conditions. Formation of pyrrolyl-thiophenes are observed only in the reactions of nitrothiophenes with isoprene.
sciforum-000414	Isoprene-mediated lithiation of chiral N-alkylimidazoles Rosario Torregrosa , Isidro Pastor , Miguel Yus Submitted: 29 Nov 2007 Abstract: Show Abstract	Rosario Torregrosa , Isidro Pastor , Miguel Yus	N/A	Show Abstract
The isoprene-mediated lithiation of different chiral N-alkylimidazoles (2a and 2b) and the following reaction with pivalaldehyde leads to the corresponding imidazolylpropanol derivatives 4 and 5 with excellent overall yield, but low de (up to 26%).