The 4th International Electronic Conference on Synthetic Organic Chemistry
Part of the Electronic Conference on Synthetic Organic Chemistry series
1–30 Nov 2000
Call for Papers
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.
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.
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).
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 | Presentation | ||||||||||||||||||||||||||||||||||||||
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sciforum-000932 |
Synthesis and Study of Polyelectrolytes on the Basis of Glycidyl Ester of Methacrylic Acid
, Edyl Ergozhin ,
Nazira Chopabayeva ,
Karlygash Bazarbayeva
Submitted: 10 Sep 2000 Abstract: Show Abstract |
,
Edyl Ergozhin ,
Nazira Chopabayeva ,
Karlygash Bazarbayeva
|
N/A |
Show Abstract |
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The synthesis of reticulated polyelectrolytes possessing ion-exchange properties, remains a topical task in chemistry. The constant widening of the application fields of such polymers in experimental studies and industry stipulates a more and more increasing interest to the problem of their preparation. | |||||||||||||||||||||||||||||||||||||||||
sciforum-000971 |
Isolation and Biological Activity of the Oligostilbenes of Cyphostemma Crotalarioides
A. Bala ,
R. Delorme ,
A. Kollmann ,
L. Kerhoas ,
J. Einhorn ,
Submitted: 10 Sep 2000 Abstract: Show Abstract |
A. Bala ,
R. Delorme ,
A. Kollmann ,
L. Kerhoas ,
J. Einhorn ,
|
N/A |
Show Abstract |
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In our on-going programs aimed to the discovery of new pesticides of plant origin, we have extensively studied the composition in secondary metabolites of various indigenous plants from the Sudan, known for their promising biological activity and sometimes even used in traditional agriculture for pest management purposes. | |||||||||||||||||||||||||||||||||||||||||
sciforum-000903 | 3-(2,5-Cyclohexadienyl)-L-alanine (1,4-Dihydro-L-phenylalanine) - Its Synthesis and Behaviour in the Phenylalanine Ammonia-Lyase Reaction | , | N/A |
Show Abstract |
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The title compound was synthesised by the reduction of L-phenylalanine with lithium in liquid ammonia. Consistent with the Birch rule the main product was 2,5-dihydro-L-phenylalanine. 1,4-dihydro-L-phenylalanine was isolated by HPLC on a reversed phase column and characterised as a minor product of the Birch reduction. Both dihydro-L-phenylalanines were assayed in the phenylalanine ammonia-lyase (PAL) reaction. 2,5-Dihydro-L-phenylalanine was a substrate for PAL with Km about one third and Vmax 30 times less than that of the values of the natural substrate L-phenylalanine and converted into the corresponding 2,5-dihydrocinnamic acid. On the other hand 1,4-dihydro-L-phenylalanine was not converted by PAL. Both isomers were, however, competitive inhibitors of the enzymatic reaction. The Ki value of 1,4-dihydro-L-phenylalanine was 5.1 times higher as with the 2,5-dihydro isomer. These results support the proposed mechanism of the PAL reaction starting with an electrophilic attack of the 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO) prosthetic group at the ortho position of the phenyl ring of the substrate. | |||||||||||||||||||||||||||||||||||||||||
sciforum-001009 | Synthesis of 1-(2'-Deoxy-ß-D-ribofuranosyl)-1H-imidazo[4,5-d]pyridazine-4,7(5 H,6H)-dion: a Potentially Beneficial Building Block for Antisense Applications |
Huan-Ming Chen ,
|
N/A |
Show Abstract |
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Synthesis of the title compound,1-(2'-deoxy-ß-D-ribofuranosyl)-1H-imidazo[4,5-d]pyridazine- -4,7(5H,6H)-dione (1), is reported. It was synthesized in five steps, commencing with methyl 1-(ß-D-ribofuranosyl)imidazo-4,5-dicarboxylate (2). The 3',5'-hydroxyl groups of 2 was protected with a bis-silylating agent to form 3, which was then converted into the corresponding 2'-thionocarbonate derivative 5. The reduction of the latter with tri-n-butyltin hydride (to form 6), followed by silyl deprotection with tetra-n-btylammonium fluoride, afforded 7. Treatment of the latter with hydrazine hydrate yielded the target nucleoside 1. | |||||||||||||||||||||||||||||||||||||||||
sciforum-000998 | Brief Synthesis of the Cell Cycle Inhibitor Tryprostatin B and Its Alanine Analogue |
Esmeralda Caballero ,
Carmen Avendaño ,
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N/A |
Show Abstract |
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Tryprostatin B and its analogue containing alanine instead of proline were synthesized from cyclo-(L-Trp-L-Pro) and cyclo-(L-Trp-L-Ala), respectively, by tandem C-3 prenylation/cyclization, followed by acid-catalyzed migration of the prenyl group to the indole C2 position. |
List of Authors (153)
Mohamed Abass
Karl-Heinz Altmann
Uwe Beifuss
Matthias Beller
Michele Bertrand
Stefan Bienz
I. Bischoff
Christian Bochet
Alberto Brandi
Stefan Bräse
Jean Brunel
Gloria Brusotti
Vladimir Bulavka
Sandro Cacchi
Marina Caldarelli
Christian Chapuis
Ruzena Cizmarikova
Matteo Conza
Sergiu Coseri
Raquel Cravero
Norbert De Kimpe
Paola Del Buttero
Christian Dreyer
Annelies Eeckhaut
Jacques Einhorn
Olivér Éliás
Lothar Elling
K. Faber
Mohamed Abass
Karl-Heinz Altmann
Uwe Beifuss
Matthias Beller
Michele Bertrand
Stefan Bienz
I. Bischoff
Christian Bochet
Alberto Brandi
Stefan Bräse
Jean Brunel
Gloria Brusotti
Vladimir Bulavka
Sandro Cacchi
Marina Caldarelli
Christian Chapuis
Ruzena Cizmarikova
Matteo Conza
Sergiu Coseri
Raquel Cravero
Norbert De Kimpe
Paola Del Buttero
Christian Dreyer
Annelies Eeckhaut
Jacques Einhorn
Olivér Éliás
Lothar Elling
K. Faber
D. Feineis
Eduard Felder
Habib Firouzabadi
S. Furegati
Guido Galley
Armin Geyer
Serafino Gladiali
David Goldsmith
Jörg Habermann
Hisahiro Hagiwara
Jens Hartung
M. Herderich
Kevin Hodgetts
Robert Hoffman
Andrew Hughes
Heiko Ihmels
Christopher Imrie
Katsuhiko Inomata
Johann Jauch
Marjan Jeselnik
Martin Johnston
Raymond Jones
Kobe Joze
Norbert Jux
Thomas Kappe
C. Kappe
C. Kappe
Yoel Kashman
Olga Kataeva
Takeo Kawabata
U. Kazmaier
Andreas Kirschning
Györgyi Kovács
Katarina Kralova
W. Kroutil
L. Kubicova
Guillermo Labadie
Mariano Laguna
Frédéric Lamaty
Steven Ley
Guigen Li
Peter Lohse
Davor Margetic
C. Marquis
S. Mayer
Frank McDonald
Alessandro Mordini
Thomas Müller
Paul Müller
M. Münchbach
Thomas Netscher
Mario Orena
Albert Padwa
Thomas Pettus
Giovanni Poli
Gianluca Pozzi
Silvio Quici
Oleg Rakitin
Christopher Richards
Clemens Richert
John Robinson
Mark Rogozin
David Rosenberg
Carlo Rosini
Karola Rück-Braun
Floris Rutjes
Ilhyong Ryu
W. Sander
Barbara Schnell
Thomas Schrader
James Scott
Julio Seijas
M. Senge
Mathias Senge
Jose Sepulveda-Argues
Anatoly Shutalev
Lech Skulski
M. Speck
Kevin Sprott
Wolfgang Stadelbauer
Alexander Stadler
Branko Stanovnik
Thies Thiemann
Ralf Thiericke
Tomas Torroba
Michael Trzoss
Sakae Uemura
Georg Uray
M. Vázquez-Tato
Aušra Vektarienė
Gytis Vektaris
Robert Vleggaar
Marina Vogel
Ronald Warrener
P. Wessig
Bernhard Westermann
Lorenzo Williams
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
©2001 by MDPI, Basel, Switzerland
Rates for CD-ROM archive edition
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CHF 150 after the conference
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A. General Organic Synthesis
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B. Solid Phase Chemistry and Combinatorial Synthesis
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C. Bioorganic Chemistry and Natural Products
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