The 4th International Electronic Conference on Synthetic Organic Chemistry

Part of the Electronic Conference on Synthetic Organic Chemistry series

Call for Papers

Name: The 4th International Electronic Conference on Synthetic Organic Chemistry
Start: 2000-10-31T23:00:00
End: 2000-11-29T23:00:00

This will be the 4th 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. Solid Phase Chemistry and Combinatorial Synthesis
C. Bioorganic Chemistry and Natural Products

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 (151)

Id	Title	Authors	Poster PDF
sciforum-000842	New heterocyclic materials Tomas Torroba , Oleg Rakitin , Charles Rees Submitted: 10 Sep 2000 Abstract: Show Abstract	Tomas Torroba , Oleg Rakitin , Charles Rees	N/A	Show Abstract
The preparation of new heterocyclic systems by conventional ways is normally a hard work that implies many synthetic steps and expensive starting materials. Even more, many heterocyclic systems, being predictably stable, are impossible to be prepared because the synthetic approach simply does not exist. There is a very different approach to get new heterocyclic systems that uses simple organic starting materials (tertiary amines, alicyclic oximes) bearing a nucleophilic nitrogen which generates reactive intermediates, subsequently trapped by a inorganic reagent, disulfur dichloride (S2Cl2). In general, trapping of intermediates is followed by extensive dehydrogenation and chlorination to give new intermediates that can be trapped by selected nucleophiles on the way to stable final products.1-2 A good combination of reagents and reaction sequences permits the preparation of heterocycles that imply up to fifteen different steps all working sequentially in a one-pot reaction. The best example of this chemistry is the reaction of N-ethyldiisopropylamine (Hünig’s base), with disulfur dichloride.3-4 The first step is a slow oxidation of the amine to an immonium salt by a combination of disulfur dichloride and DABCO (diazabicyclo[2.2.2]octane).
sciforum-000843	Synthesis of Polycyclic Ring Systems Using Transition Metal Catalyzed Cyclizations of Diazo Alkynyl Ketones Albert Padwa Submitted: 10 Sep 2000 Abstract: Show Abstract	Albert Padwa	N/A	Show Abstract
The rhodium(II)-catalyzed reaction of a-diazo ketones bearing tethered alkyne units represents a new and useful method for the construction of a variety of substituted cyclopentenones. The process proceeds by addition of the rhodium-stabilized carbenoid onto the acetylenic pi-bond to give a vinyl carbenoid intermediate. The resulting rhodium complex undergoes a wide assortment of reactions including cyclopropanation, 1,2-hydrogen migration, CHinsertion, addition to tethered alkynes and ylide formation. When 2-alkynyl-2-diazo-3-oxobutanoates were treated with a Rh(II)-catalyst, furo[3,4-c]furans were formed in excellent yield.
sciforum-000844	3-Dimethylaminopropenoates and Related Compounds in the Synthesis of Heterocyclic Systems and Heterocyclic Amino Acids Branko Stanovnik Submitted: 10 Sep 2000 Abstract: Show Abstract	Branko Stanovnik	N/A	Show Abstract
a -Amino and a -hydroxy acids and their derivatives play an important role in organic synthesis, especially in asymmetric synthesis as chiral synthons, chiral auxiliaries, and resolving agents [1-3]. In the course of our studies of heteroaryl substituted a -amino and a -hydroxy acids and their derivatives we have prepared easily accessible 2-acylamino-3-dimethylaminopropenoates, 2-(O-substituted hydroxy)-3- dimethylaminopropenoates, and 2-ethenylamino-3-dimethylaminopropenoates, masked a -formyl-a -amino- and a - formyl-a -hydroxy acids, and their derivatives. They have turned out to be excellent reagents for the preparaton of a variety of heterocyclic systems with an amino or hydroxy acid structural element incorporated or partially incorporated into the newly formed heterocyclic ring [4]
sciforum-000845	Organic Iodine(I, III, and V) Chemistry: 10 Years of Development at the Medical University of Warsaw, Poland Lech Skulski Submitted: 10 Sep 2000 Abstract: Show Abstract	Lech Skulski	N/A	Show Abstract
This review reports some novel (or considerably improved) methods of the synthesis of aromatic iodides, (dichloroiodo)arenes, (diacetoxyiodo)arenes, iodylarenes, diaryliodonium salts as well as some facile, oxidative anion metatheses in crude diaryliodonium halides and, for comparison, potassium halides. All these new results were obtained in our laboratory within the past decade (1990- 2000). A full list of our papers dealing with the organic iodine(I, III and V) chemistry, covering exlusively the aromatic derivatives, is also submitted (Refs. 1-18)
sciforum-000846	Preparation of new enantiopure atropisomeric b-aminoalcohols and their use in asymmetric catalysis: enantioselective addition of diethylzinc to aromatic aldehydes. Tommaso Mecca , Stefano Superchi , Carlo Rosini Submitted: 10 Sep 2000 Abstract: Show Abstract	Tommaso Mecca , Stefano Superchi , Carlo Rosini	N/A	Show Abstract
A new class of enantiopure b-aminoalcohols having 1,1’-binaphthyl skeleton, and chiral only by atropisomerism, has been prepared and tested as catalytic precursors in the asymmetric addition of diethylzinc to aromatic aldehydes. The aldehydes were quickly and cleanly (99% yield) transformed in the corresponding alcohols with ee up to 87%.

Full List

List of Authors (153)

Mohamed Abass

Karl-Heinz Altmann

Annette Beck-Sickinger

Uwe Beifuss

Nesipkhan Bektenov

Matthias Beller

Michele Bertrand

Stefan Bienz

I. Bischoff

Christian Bochet

Alberto Brandi

Stefan Bräse

Jean Brunel

Gloria Brusotti

Vladimir Bulavka

Sandro Cacchi

Dominique Cahard

Marina Caldarelli

Srinivasan Chandrasekaran

Christian Chapuis

Ruzena Cizmarikova

Matteo Conza

Sergiu Coseri

Raquel Cravero

Norbert De Kimpe

Paola Del Buttero

Jerry Dias

Martin Dolezal

Christian Dreyer

P. Ducrot

Annelies Eeckhaut

Jacques Einhorn

Olivér Éliás

Lothar Elling

Jean Jacques Eynde

K. Faber

Mohamed Abass

Karl-Heinz Altmann

Annette Beck-Sickinger

Uwe Beifuss

Nesipkhan Bektenov

Matthias Beller

Michele Bertrand

Stefan Bienz

I. Bischoff

Christian Bochet

Alberto Brandi

Stefan Bräse

Jean Brunel

Gloria Brusotti

Vladimir Bulavka

Sandro Cacchi

Dominique Cahard

Marina Caldarelli

Srinivasan Chandrasekaran

Christian Chapuis

Ruzena Cizmarikova

Matteo Conza

Sergiu Coseri

Raquel Cravero

Norbert De Kimpe

Paola Del Buttero

Jerry Dias

Martin Dolezal

Christian Dreyer

P. Ducrot

Annelies Eeckhaut

Jacques Einhorn

Olivér Éliás

Lothar Elling

Jean Jacques Eynde

K. Faber

D. Feineis

Eduard Felder

Habib Firouzabadi

Christopher Frost

S. Furegati

Guido Galley

Armin Geyer

Serafino Gladiali

David Goldsmith

Jörg Habermann

Hisahiro Hagiwara

Serkos Haroutounian

Jens Hartung

M. Herderich

Kevin Hodgetts

Robert Hoffman

Ramachandra Hosmane

Andrew Hughes

Heiko Ihmels

Christopher Imrie

Katsuhiko Inomata

Johann Jauch

Marjan Jeselnik

Martin Johnston

Raymond Jones

Kobe Joze

Norbert Jux

Shuji Kanemasa

C. Kappe

Thomas Kappe

C. Kappe

Yoel Kashman

Olga Kataeva

Takeo Kawabata

U. Kazmaier

Andreas Kirschning

Lajos Kovács

Györgyi Kovács

Katarina Kralova

George Kraus

W. Kroutil

L. Kubicova

Guillermo Labadie

Mariano Laguna

Frédéric Lamaty

Steven Ley

Guigen Li

Peter Lohse

Amedea Manfredi

Davor Margetic

C. Marquis

S. Mayer

Frank McDonald

J. Menéndez

Pedro Merino

Alessandro Mordini

Paul Müller

Thomas Müller

M. Münchbach

Carmen Najera

Thomas Netscher

Mario Orena

Albert Padwa

Thomas Pettus

Giovanni Poli

Gianluca Pozzi

Silvio Quici

Oleg Rakitin

János Rétey

Christopher Richards

Clemens Richert

John Robinson

Mark Rogozin

David Rosenberg

Carlo Rosini

Karola Rück-Braun

P. Rüedi

Floris Rutjes

Ilhyong Ryu

W. Sander

Barbara Schnell

Thomas Schrader

James Scott

Julio Seijas

Mathias Senge

M. Senge

Jose Sepulveda-Argues

Anatoly Shutalev

Alexander Skolaut

Lech Skulski

M. Speck

Kevin Sprott

Wolfgang Stadelbauer

Alexander Stadler

Branko Stanovnik

Thies Thiemann

Ralf Thiericke

M. Tiecco

Francisco Torrens

Tomas Torroba

Michael Trzoss

Sakae Uemura

Kjell Undheim

Georg Uray

M. Vázquez-Tato

Aušra Vektarienė

Gytis Vektaris

Robert Vleggaar

Marina Vogel

Ronald Warrener

P. Wessig

Bernhard Westermann

Lorenzo Williams

M. Yus

Matteo Zanda

Alexander Zapf

Proceedings & Editors

Editors

Thomas Wirth

C. Oliver Kappe

Eduard Felder

Ulf Diederichsen

Shu-Kun Lin

CD-ROM edition

ISBN: 3-906980-05-7

Published in 2001 by MDPI, Basel, Switzerland

Rates for CD-ROM archive edition

CHF 100 before the conference

CHF 150 after the conference

CHF 250 per year for non-participants and for institutions

Please place the order by e-mail: Billing

The 4th International Electronic Conference on Synthetic Organic Chemistry

Part of the Electronic Conference on Synthetic Organic Chemistry series

1–30 November 2000

Call for Papers

Sessions

Instructions for Authors

List of accepted submissions (151)

List of Authors (153)

Proceedings & Editors

A. General Organic Synthesis

Submissions

B. Solid Phase Chemistry and Combinatorial Synthesis

Submissions

C. Bioorganic Chemistry and Natural Products

Submissions