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Table of Contents

Molecules, Volume 5, Issue 9 (September 2000), Pages 1055-1079

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	p. 1055-1061 Hui-Ling Liu, Zongcheng Lieberzeit and Thorleif Anthonsen Article: Synthesis and Fungicidal Activity of 2-Imino-3-(4-arylthiazol-2-yl)-thiazolidin-4-ones and Their 5-Arylidene Derivatives Molecules 2000, 5(9), 1055-1061; doi:10.3390/50901055 Received: 15 August 2000 / Accepted: 29 August 2000 / Published: 5 September 2000 Show/Hide Abstract | Download PDF Full-text (32 KB) Abstract: Five derivatives of 2-imino-3-(4-arylthiazol-2-yl)-thiazolidin-4-ones and a series of their 5-arylidene derivatives have been synthesized and tested for antifungal activity against seven agricultural fungi. 2-Imino-3-(2,4-dichloro-5-fluorophenylthiazol-2-yl)-4-thiazolidi-none and 2-imino-3-(2,4-dichlorophenylthiazol-2-yl)-4-thiazolidione, both of them new compounds, exhibited higher fungicidal effects than the other compounds prepared.
	p. 1062-1067 Tomoshige Kobayashi and Sayuri Kobayashi Article: Swern Oxidation of Bicyclo[2.2.1]hept-5-ene-2,3-diol and Its Pyrazine-fused Derivatives: An Improved Synthesis of Bicyclo[2.2.1]hept-5-ene-2,3-dione and An Unexpected Ring-Opening Reaction Molecules 2000, 5(9), 1062-1067; doi:10.3390/50901062 Received: 14 August 2000 / Accepted: 6 September 2000 / Published: 9 September 2000 Show/Hide Abstract | Download PDF Full-text (35 KB) Abstract: An improved synthesis of bicyclo[2.2.1]hept-5-ene-2,3-dione by Swern oxidation of bicyclo[2.2.1]hept-5-ene-2,3-diol, and an unexpected ring-opening reaction by the Swern oxidation of pyrazine-fused congeners are described.
	p. 1068-1079 Eduardo F. Córsico, Al Postigo and Roberto A. Rossi Review: Recent Advances in the Substitution Reactions of Triorganylstannyl Ions with Aromatic Compounds by the SRN1 Mechanism. Synthetic Applications Molecules 2000, 5(9), 1068-1079; doi:10.3390/50901068 Received: 30 May 2000; in revised form: 18 August 2000 / Accepted: 5 September 2000 / Published: 11 September 2000 Show/Hide Abstract | Download PDF Full-text (65 KB) Abstract: A review on the reactions of triorganyl stannyl ions with haloarenes is presented. Emphasis on the synthetic applications of the resulting triorganyl stannyl aryl compounds is made, with their inherent potential to build large molecules through the SRN1 sequence, i.e. ArX→ArSnR3→ArAr, which can be iteratively repeated when appropriately substituted substrates are chosen.
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