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71.
The synthesis of C8-glycomimetics is described from C2-symmetrical polyhydroxylated cyclooctenes derived from carbocyclisation of enantiomerically pure 1,9-dienes by ring closing metathesis. Their obtention notably involved either hydroboration followed by oxidation to carbasugars or to cyclooctanones then reductive amination, or formation of a cis-cyclic sulfate followed by successive introduction of an azido group, reduction and subsequent reductive amination. The biological activity of the C8-carbasugars and related aminocyclitols, analogous to voglibose, has been evaluated towards several commercially available glycosidases. 相似文献
72.
J. J. Tondeur G. Vandendunghen M. Watelet 《Reaction Kinetics and Catalysis Letters》1988,36(1):125-129
We have studied the kinetics of the reaction of L-hydroxyproline with OCH(CH2)6NCO, catalyzed by organotin, avoiding side reactions by protecting the other active hydrogens of the aminoacid, and comparing it with the MeOH/n-BuNCO system.
L-- -OCN(CH2)6NCO, , . . - .相似文献
73.
Constable EC Figgemeier E Housecroft CE Olsson J Zimmermann YC 《Dalton transactions (Cambridge, England : 2003)》2004,(13):1918-1927
The synthesis and electronic properties of dinuclear ([(bipy)2Ru(I)M(terpy)][PF6]4(bipy = 2,2'-bipyridine, terpy = 2,2':6',2'-terpyridine; M = Ru, Os)) and trinuclear ([[(bipy)2Ru(I)]2M][PF6]6 M = Ru, Os, Fe, Co) complexes bridged by 4'-(2,2'-bipyridin-4-yl)-2,2':6',2'-terpyridine (I) have been investigated and are compared with those of mononuclear model complexes. The electrochemical analysis using cyclic voltammetry and differential pulse voltammetry reveals that there are no interactions in the ground state between adjacent metal centres. However, there is strong electronic communication between the 2,2'-bipyridine and 2,2':6',2'-terpyridine components of the bridging ligand. This conclusion is supported by a step-by-step reduction of the dinuclear and trinuclear complexes and the assignment of each electrochemical process to localised ligand sites within the didentate and terdentate domains. The investigation of the electronic absorption and emission spectra reveals an energy transfer in the excited state from the terminating bipy-bound metal centres to the central terpy-bound metal centre. This indicates that the bridge is able to facilitate energy transfer in the excited state between the metal centres despite the lack of interactions in the ground state. 相似文献
74.
Nitrosyl chloride is only chlorinating in darkness and above 100°. In the sun light and at room temperature it reacts as a chlorinating, nitrosating, nitrating and oxidizing agent. With trichlorethylene in fact pentachlorethane 1,1,1,2-tetrachloro-2-nitrosoethane, 1,1,1,2-tetrachloro-2-nitroethane, dichloracetic acid and a compound of empirical formula C4H2Cl5NO2 are obtained. Tetrachloroethylene carried to hexachlorethane, pentachloronitrosoethane and tetrachloro-2-(pentachlorethyl)-1,2-oxazetidine. Introduced nitrosyl chloride provided nitrogen monoxide prouved by gaz chromatography. This monoxide reacted afterwards to give nitrogen which is the single nitrogenous gazeous compound. Carbondioxide is a minor component of the gaz. 相似文献
75.
Trombotto S Danel M Fitremann J Bouchu A Queneau Y 《The Journal of organic chemistry》2003,68(17):6672-6678
The base-catalyzed reaction of carboxymethyl 3,4,6-tri-O-acetyl-alpha-D-glucopyranoside 2-O-lactone (prepared from isomaltulose) with amino acids and fatty amines under basic catalysis gave a series of new pseudoglucopeptides, nonionic amphiphiles, and polymerizable derivatives. The same reaction applied to alcohols provided the corresponding 2-(alpha-D-glucopyranosyloxy)acetyl esters with either basic or acidic catalysts. 相似文献
76.
Laurent Salvi Hélène Cattey Yves Mugnier Antonio Otero 《Journal of organometallic chemistry》2004,689(22):3473-3480
Electrochemical reduction of niobocene dichloride (η5-C5H4SiMe3)2NbCl21 formulated as in the presence of 3,4-diaminobenzoic acid yields to the complex [Nb(η5-C5H4SiMe3)2(κ2-O,O-OOC(C6H3)(NH2)2)] 3. When CN(2,6-Me2C6H3) formulated as xylylisonitrile (CNXylyl) is added to a complex 3 solution, a substitution reaction takes place to lead to the complex [Nb(η5-C5H4SiMe3)2(κ1-O-OOC(C6H3)(NH2)2)(CN(2,6-Me2C6H3)) 4 after 3 h. An alternative way to yield quantitatively and nearly instantaneously 4 consists in a previous oxidation of 3 in the presence of CNXylyl. Hence, we present here a new example of electron-transfer-catalyzed (ETC) ligand substitution of carboxylato niobocene complex induced by electrochemical oxidation. The structure of the complexes, the formation mechanism are described using electrochemical and spectroscopic data. Electrochemical simulation have been done to verify experimental results and to complete them with a kinetic study. 相似文献
77.
The water exchange of [V(H2O)6]Cl2 in aqueous solution has been studied as a function of temperature and pressure (up to 250 MPa), by measuring the 17O-FT-NMR. line-widths of the free water resonance at 8.13 MHz. The kinetic parameters obtained are K = 87±4 s?1, ΔH* = +61.8 ± 0.7 kJ mo1?1 and ΔS* = ?0.4±1.9 J mol?1 K?1. A pressure-independent volume of activation ΔV* = ?4.1±0.1 cm3 mol?1 is obtained, suggesting an associative interchange (Ia) mechanism for this early divalent metal ion. 相似文献
78.
Yves Le Jan 《Comptes Rendus Mathematique》2012,350(13-14):643-646
We study the clusters defined by Poisson processes of Markov loops. 相似文献
79.
Yves Crama Michel Grabisch Silvano Martello 《4OR: A Quarterly Journal of Operations Research》2016,14(4):333-336
We recall some cases of ethical misconduct that occurred in the recent years, and we report a new trick that was recently attempted to cheat the journal in order to obtain the publication of an article through usurped identity. 相似文献