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Showing papers in "Journal of Chemical Research-s in 1990"






Journal Article
TL;DR: Zinc iodide in the presence of acylating agents such as carboxylic acid anhydrides and chlorides cleaves alkyl and benzyl ethers efficiently under mild conditions as discussed by the authors.
Abstract: Zinc iodide in the presence of acylating agents such as carboxylic acid anhydrides and chlorides cleaves alkyl and benzyl ethers efficiently under mild conditions

4 citations





Journal Article
TL;DR: La synthese s'effectue a partir du chlorure de benzoyle ou de l'N-(α-alkyltellurobenzylidene) p-toluenesulfonamide, et de l'shydrogenotellurure de sodium.
Abstract: La synthese s'effectue a partir du chlorure de benzoyle ou de l'N-(α-alkyltellurobenzylidene) p-toluenesulfonamide, et de l'hydrogenotellurure de sodium

3 citations


Journal ArticleDOI
TL;DR: In this paper, the authors present a scheme for the detection of chemical properties in the presence of chemical molecules, and apply it to chemical properties of the chemical compounds. http://hdl.handle.net/10261/16430
Abstract: 2 pages, 1 scheme.-- Paper in Journal of Chemical Research(M) available at: http://hdl.handle.net/10261/16430

3 citations




Journal Article
TL;DR: In this article, a potentiometric investigation (glass electrode) on the protonation of ethylenediamine in LiCl, NaCl, KCl, NNO 3, NaClO 4, MgCl 2, CaCl 2, Me 4 NCl, and Et 4 NI was conducted.
Abstract: We report a potentiometric investigation (glass electrode) on the protonation of ethylenediamine in LiCl, NaCl, KCl, NaNO 3 , NaClO 4 , MgCl 2 , CaCl 2 , Me 4 NCl, and Et 4 NI (Me 4 N + and Et 4 N + are tetramethylammonium and tetraethylammonium cations respectively) at T=25 o C. The literature on the protonation of ethylenediamine 11 was also examined


Journal Article
TL;DR: Sodium dithionite is shown to be a useful reagent for the reductive desulphonation of acyl sulphones under mild conditions which should be readily applicable to large scale synthesis.
Abstract: Sodium dithionite is shown to be a useful reagent for the reductive desulphonation of acyl sulphones under mild conditions which should be readily applicable to large scale synthesis


Journal Article
TL;DR: The meilleure methode est celle ou l'on fait reagir le bis-[hydroxy-2p ethoxy]-1,2 benzene avec le ditosylate de l'oligoethylene glycol, en presence d'hydrure de sodium, dans le THF as discussed by the authors.
Abstract: La meilleure methode est celle ou l'on fait reagir le bis-[hydroxy-2p ethoxy]-1,2 benzene avec le ditosylate de l'oligoethylene glycol, en presence d'hydrure de sodium, dans le THF

Journal Article
TL;DR: A simple and general method for the synthesis of diaroyl diselenides involves reaction of selenium with sodium hydroxide at 65-70 o C and under phase-transfer conditions to give sodium diselsenide, which reacts with aroyl chlorides to afford the diaroyl disels in good to excellent isolated yields as discussed by the authors.
Abstract: A simple and general method for the synthesis of diaroyl diselenides involves reaction of selenium with sodium hydroxide at 65-70 o C and under phase-transfer conditions to give sodium diselenide, which reacts with aroyl chlorides to afford the diaroyl diselenides in good to excellent isolated yields



Journal Article
TL;DR: In this article, Me 2 N−CH=N―A is considered as iminologues of compounds Me 2 n−A and it is shown that iminology extends significantly the range of hydrogen-bond basicities of nitriles, thioamides, and sulphonamides.
Abstract: Compounds Me 2 N―CH=N―A are considered as iminologues of compounds Me 2 N―A and it is shown that iminology extends significantly the range of hydrogen-bond basicities of nitriles, thioamides, and sulphonamides


Journal Article
TL;DR: A novel flavone glycoside, designated as infectoriin, has been isolated from the leaves of Ficus infectoria (Moraceae) and has been assigned the structure 1 on the basis of chemical and spectral evidence as mentioned in this paper.
Abstract: A novel flavone glycoside, designated as infectoriin, has been isolated from the leaves of Ficus infectoria (Moraceae) and has been assigned the structure 1 on the basis of chemical and spectral evidence

Journal Article
TL;DR: A novel method of regiospecific τ-im-alkylation and also cyclopeptide synthesis via 2-hydroxyphenyl esters is described, exemplifying a novel way to synthesise thyroliberin analogues with different racemates.
Abstract: Syntheses of the bridged thyroliberin analogues pyroglutamyl-cyclo-Nτ-(6-aminohexyl) histidylproline (1a) and pyroglutamyl-cyclo-Nτ-(5-aminopentyl) histidylproline (1b) are described, exemplifying a novel method of regiospecific τ-im-alkylation and also cyclopeptide synthesis via 2-hydroxyphenyl esters