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931.
H. Schumann 《Angewandte Chemie (International ed. in English)》1969,8(12):937-950
The preparation, properties, and reactions of the compounds named in the title are described, with particular reference to the possible participation of (p→d)π components in the bonding between the group IVB and the group VB elements. 相似文献
932.
Grzegorz Mlosto Jaroslaw Romaski Anthony Linden Heinz Heimgartner 《Helvetica chimica acta》1995,78(5):1067-1078
First Example of an H-Shift in ‘Thiocarbonyl Aminides’ (N-(Alkylidenesulfonio)aminides) Reaction of benzyl azide ( 15a ) with the sterically hindered C?S group of 4,4-dimethyl-1,3-thiazole-5(4H)-thiones 14 (Scheme 3) and 1,1,3,3-tetramethylindane-2-thione ( 17 , Scheme 4) at 80° leads to the corresponding imines in high yield, without formation of any by-product. In contrast, 15a and 2,2,4,4-tetramethyl-3-thioxocyclobutanone ( 7 ) under the same conditions yielded, in addition to imine 19 , products 20a and 21 (Scheme 5). For the formation of 20a , a reaction mechanism via [1,4]-H shift in the intermediate ‘thiocarbonyl aminides’ 23 is proposed (Scheme 6). Product 21 as well as the dithiazole derivative 22 , which is formed only in the reaction with 4-nitrobenzyl azide ( 15c ), are formal adducts of the dipole 23 . Whereas precedents are known for the formation of cycloadducts of type 22 , the pathway to 21 is not known. Two possible mechanisms of its formation are proposed in Schemes 8 and 9. 相似文献
933.
Adrenaline, noradrenaline, 3,4-dihydroxyphenylalanine (Dopa) and adrenaline plus noradrenaline as total catecholamines can automaticallyfluorimetrically be determined in one analysis system (according to Wisser) by the trihydroxyindole method. The fluorescence yields for the fluorophores of the single compounds are dependent on the pump speed of the autoanalyzer except for the differentiated determination of adrenaline. Caused by these differences effects of selectivity are demonstrated for the determination of Dopa disturbed by noradrenaline and adrenaline disturbed by noradrenaline. Also the influence of the suction time on the fluorescence yield was investigated. The optimal adjustings for the single methods of determination are given. 相似文献
934.
935.
Three classes of monosubstituted carbenes (aryl-, vinyl-, carbonyl-) and one class of disubstituted carbenes (dicarbonyl-), all of them ground state triplets, can exist in more than one rotameric form with distinct zero field splitting parameters. Representative examples of these carbenes are discussed and selected aspects of triplet carbenes are evaluated, including their π spin density distribution, intramolecular H-abstraction, and cis-trans isomerization. Lastly, the structures assigned to two triplets generated by photolysis of dibenzoyldiazomethane are re-evaluated. 相似文献
936.
Regioselective 1,3-Dipolar Cycloadditions of a ‘Thiocarbonyl-methanide’ ((Alkylidenesulfonio)methanide) with Aromatic Sulfines Reaction of the spirocyclic 2,5-dihydro-1,3,4-thiadiazole 7 and thiobenzophenone S-oxide ( 6a ) in THF at 45° yielded the spirocyclic 1,3-dithiolane 1-oxide 8 , thiirane 9 , and the diazane derivative 10 in a ratio of 61:15:23 (Scheme 2). The formation of 8 is rationalized by a 1,3-dipolar cycloaddition of ‘thiocarbonyl-methanide’ 1 , generated from 7 by thermal elimination of N2, and the C?S bond of sulfine 6a . Cyclization of intermediate 1 leads to thiirane 9 . Under the same conditions, 7 and adamantane-2-thione S-oxide ( 6b ) or 2,2,4,4-tetramethyl-3-thioxocyclobutanone S-oxide ( 4 ) reacted to give only 9 and 10 but no cycloadduct of type 8 (Scheme 4). With the aim to favor the formation of 8 , a mixture of 6a and 1.1 equiv. of 7 was heated to 45° without any solvent in a sealed tube. The ratio of products was only slightly different from that of the thermolysis in THF. An analogous experiment with 7 and 9H-fluorene-9-thione S-oxide ( 6c ) yielded cycloadduct 13 and 9 (Scheme 5). It is most interesting that the 1,3-dipolar cycloadditions of 1 and the sulfines 6a and 6c proceeded with different regioselectivity. A reaction mechanism for the unexpected formation of 10 is proposed in Scheme 7. The key step is the base-catalyzed ring opening of 7 and the nucleophilic addition of the thereby formed thiolate 21 onto the sulfonium ion 19 . 相似文献
937.
Karl-Richard Meier Anthony Linden Heinz Heimgartner Grzegorz Mlosto 《Helvetica chimica acta》1997,80(4):1190-1204
1,3-Dipolar Cycloadditions of a Carhonyl-ylide with 1,3-Thiazole-5(4H)-thiones and Thioketones Inp-xylene at 150°, 3-phenyloxirane-2,2-dicarbonitrile ( 4b ) and 2-phenyl-3-thia-1-azaspiro[4.4]non-1-ene-4-thione ( 1a ) gave the three 1:1 adduets trans- 3a , cis- 3a , and 13a in 61, 21, and 3% yield, respectively (Scheme 3). The stereoisomers trans- 3a and cis- 3a are the products of a regioselective 1,3-dipolar cycloaddition of carbonylylide 2b , generated thermally by an electrocyclic ring opening of 4b (Scheme 6), and the C?S group of 1a . Surprisingly, 13a proved not to be a regioisomeric cycloadduct of 1a and 2b , but an isomer formed via cleavage of the O? C(3) bond of the oxirane 4b . A reaction mechanism rationalizing the formation of 13a is proposed in Scheme 6. Analogous results were obtained from the reaction of 4b and 4,4-dimethyl-2-phenyl-1,3-thiazole-5 (4H)-thione ( 1b , Scheme 3). The thermolysis of 4b in p-xylene at 130° in the presence of adamantine–thione ( 10 ) led to two isomeric 1:1 adducts 15 and 16 in a ratio of ca. 2:1, however, in low yield (Scheme 4). Most likely the products are again formed viathe two competing reaction mechanisms depicted in Scheme 6. The analogous reactions of 4b with 2,2,4,4-tetramethylcyclobutane-1,3-thione ( 11 ) and 9H-xanthene-9-thione ( 12 ) yielded a single 1:1 adduct in each case (Schemes). In the former case, spirocyclic 1,3-oxathiolane 17 , the product of the 1,3-dipolar cycloaddition with 2a corresponding to 3a , was isolated in only 11 % yield. It is remarkable that no 2:1 adduct was formed even in the presence of an excess of 4b. In contrast, 4b and 12 reacted smoothly to give 18 in 81 % yield; no cycloadduct of the carbonylylide 2a could be detected. The structures of cis- 3a , 13a , 15 , and 18 , as well as the structure of 14 , which is a derivative of trans- 3a , have been established by X-ray crystallography (Figs. 1–3, Table). 相似文献
938.
Reaction of 3-Amino-2H-azirines with Salicylohydrazide 3-Amino-2H-azirines 1a–g react with salicylohydrazide ( 7 ) in MeCN at 80° to give 2H, 5H-1,2,4-triazines 10 , 1,3,4-oxadiazoles 12 and, in the case of 1d , 1,2,4-triazin-6-one 11a (Scheme 3). The precursor of these heterocycles, the amidrazone of type 9 , except for 9c and 9g , which could not be isolated, has been found as the main product after reaction of 1 and 7 in MeCN at room temperature. 3-(N-Methyl-N-phenylamino)-2-phenyl-2H-azirin ( 1g ) reacts with 7 to give mainly the aromatic triazines 15b1 and 15b2 . In this case, two unexpected by-products, 16 and salicylamide ( 17 ), occurred, probably by disproportionation of a 1:1 adduct from 1g and 7 (Scheme 8). Oxidation of 10f with DDQ leads to the triazine 15a . The structure of 10c, 11a, 12c, 13 (by-product in the reaction of 1b and 7 ), the N′-phenylureido derivative 14 of 9d (Scheme 4) as well as 15b2 has been established by X-ray crystallography. The ratio of 10/12 as a function of substitution pattern in 1 and solvent has been investigated (Tables 1, 3, 4, and 7). A mechanism for the formation of 10 and 12 is proposed in Scheme 7. 相似文献
939.
Solid-solute phase equilibria in aqueous solutions,VIII: The standard gibbs energy of La2(CO3)3·8H2O
Anh Mai Nguyen Erich Königsberger Harald Marhold Heinz Gamsjäger 《Monatshefte für Chemie / Chemical Monthly》1993,124(10):1011-1018
The solubilities of lanthanum carbonate La2(CO3)3·8H2O in solutionsS
0([H+]=H mol kg–1, [Na+]=(I–H) mol kg–1, [ClO
4
–
]=I mol kg–1) at various fixed partial pressures of CO2 have been investigated at 25.0 °C. The hydrogen ion molality and the total molality of La(III) ion in equilibrium with the solid phase were determined by e.m.f. and analytical methods, respectively. The stoichiometric solubility constants
相似文献
940.
Bernhard Hostettler Jean Pierre Obrecht Roland Prewo Jost H. Bieri Heinz Heimgartner 《Helvetica chimica acta》1986,69(2):298-304
5,6,7,8-Tetrahydro-4H-1,2,5-oxadiazocin-6-ones, Ring Enlargement Products from a 3-Isoxazolidinone and 3-Amino-2H-azirines 3-Dimethylamino-2H-azirines 1 and 4,4-dimethyl-3-isoxazolidinone ( 7 ) undergo already at room temperature a ring enlargement reaction to yield 5,6,7,8-tetrahydro-4H-1,2,5-oxadiazocines of type 8 . The structure of 8a has been confirmed by X-ray crystallography. The conformation of the eight-membered ring with a trans-amide group is of particular interest (Fig. 1 and 2). 相似文献
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