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91.
Asad Ali Munawar Hussain Imran Malik Alexander Villinger Christine Fischer Peter Langer 《Helvetica chimica acta》2010,93(9):1764-1772
Double Heck cross‐coupling reactions of 2,3‐ and 3,5‐dibromopyridine with various alkenes afforded the corresponding novel di(alkenyl)pyridines. The Heck reaction of 2,5‐dibromopyridine unexpectedly afforded 5,5′‐di(alkenyl)‐2,2′‐bipyridines by palladium‐catalyzed dimerization to give 5,5′‐dibromo‐2,2′‐bipyridine and subsequent twofold Heck reaction. 相似文献
92.
Jens Langer Sven Krieck Reinald Fischer Helmar Görls Matthias Westerhausen Prof. Dr. 《无机化学与普通化学杂志》2010,636(7):1190-1198
Iodide is a very soft and large anion and as such its extreme ability to be polarized leads to a flat energy surface with respect to the variation of the Ca–I distances in [(L)nCaI2] and [(L)nCa(R)I]. The influence of the donor strength and the bulkiness of the neutral coligands L on the Ca–I distances is studied. The base adducts of calcium diiodide can be isolated after the addition of L to CaI2 or from the Schlenk equilibrium after the direct synthesis of calcium powder with aryl iodides. As L the ethers diethyl ether (Et2O), tetrahydrofuran (thf), tetrahydropyran (thp), 1,2‐dimethoxyethane (dme), 18‐crown‐6 (18C6), bis(methoxyethyl)ether (diglyme), and amines tetramethylethylenediamine (tmeda), and hexamethyltriethylenetetramine (hmteta) are studied yielding the adducts [(thp)4Ca(Ph)I] ( 1a ), [(thf)4Ca(Ph)I] ( 1b ), [(dme)2(thf)Ca(Ph)I] ( 1c ), [(18C6)Ca(Ph)I] ( 1d ), and [(tmeda)2Ca(Ph)I] ( 1e ), as well as [(thp)4CaI2] ( 2a ), [(thf)4CaI2] ( 2b ), [(Et2O)4CaI2] ( 2c ), [(diglyme)(thf)2CaI2] ( 2d ), [(diglyme)(dme)CaI2] ( 2e ), [(dme)2(thf)CaI2] ( 2f ), [(18C6)CaI2] ( 2g ), [(tmeda)2CaI2] ( 2h ), and [(hmteta)CaI2] ( 2i ). For comparison reasons, [(thf)4Ca(Ph)Br] ( 3a ), [(thp)4CaBr2] ( 4a ), [(thf)4CaBr2] ( 4b ), and [(dme)2(AcOH)CaBr2] ( 4c ) with AcOH being acetic acid are included as well. The comparison shows that the coordination number of calcium itself only plays an insignificant role whereas bulkiness and donor strength of L represent the key influences. 相似文献
93.
Viktor O. Iaroshenko Verena SpecowiusKatharina Vlach Marcelo Vilches-HerreraDmytro Ostrovskyi Satenik MkrtchyanAlexander Villinger Peter Langer 《Tetrahedron》2011,67(31):5663-5677
Difluoromethyl-containing heteroannulated pyridines, pyrimidines and pyrazoles are prepared by a two step method. The regioselective cyclizations of electron-excessive aminoheterocycles, hydrazines and amidines with CF2Cl-substituted 1,3-dicarbonyl compounds provide the corresponding CF2Cl-substituted heterocycles. Subsequent radical reactions with trimethylstannane or allyltrimethylstannane gave difluoromethyl-containing heteroannulated pyridines, pyrimidines and pyrazoles, respectively. 相似文献
94.
The Suzuki-Miyaura reaction of 2,3-dibromobenzofuran with two equivalents of boronic acids gave 2,3-diarylbenzofurans. The reaction with one equivalent of arylboronic acids resulted in site-selective formation of 2-aryl-3-bromobenzofurans. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from 2,3-dibromobenzofuran in a one-pot protocol by sequential addition of two different boronic acids. 相似文献
95.
This is a survey of the papers by M. G. Krein (and his disciples) devoted to the theory of operators in spaces with an indefinite metric and its applications.Translated from Ukrainskii Matematicheskii Zhurnal, Vol. 46, Nos. 1–2, pp. 5–17, January–February, 1994. 相似文献
96.
Synthesis of 2‐Unsubstituted 1,3‐Selenazoles by Cyclization of Selenoformamide with α‐Bromocarbonyl Compounds
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Harald Below Wolf‐Diethard Pfeiffer Karlheinz Geisler Ashot S. Saghyan Christine Fischer Peter Langer 《Journal of heterocyclic chemistry》2015,52(2):592-596
2‐Unsubstituted 1,3‐selenazoles were prepared by cyclization of selenoformamide with α‐bromoacetophenones. Parent 1,3‐selenazole was prepared by cyclization of selenoformamide with α‐bromoacetaldehyde. 相似文献
97.
M. Hussain N. Thai Hung N. Abbas R. A. Khera I. Malik T. Patonay N. Kelzhanova Z. A. Abilov A. Villinger P. Langer 《Journal of heterocyclic chemistry》2015,52(2):497-505
Arylated benzofurans were prepared by regioselective Suzuki–Miyaura cross‐coupling reactions of 2,3‐dibromobenzofuran. The reactions proceeded with very good site‐selectivity in favor of the more electron deficient position 2. The Suzuki–Miyaura reactions of 2,3,5‐tribromobenzofuran also proceeded in favor of position 2. 相似文献
98.
Unexpected Ring Enlargement of 2‐Hydrazono‐2,3‐dihydro‐1,3‐thiazoles to 1,3,4‐Thiadiazines
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Wolf‐Diethard Pfeiffer Klaus‐Dieter Ahlers Ashot S. Saghyan Alexander Villinger Peter Langer 《Helvetica chimica acta》2014,97(1):76-87
The cyclization of thiosemicarbazide with α‐bromoacetophenone can result in the formation of isomeric 1,3,4‐thiadiazines and two different thiazoles. We studied the use of 4‐methyl‐ and 4‐ethylthiosemicarbazide as dinucleophilic building blocks. In this context, we observed an unprecedented rearrangement of a 2‐hydrazono‐2,3‐dihydrothiazole to a 1,3,4‐thiadiazine. While ring contractions of 1,3,4‐thiadiazines to thiazoles are quite common, ring enlargements are new. The course of the reaction depends on the substitution pattern of the substrate. 相似文献
99.
Cyclization of 4‐Phenylthiosemicarbazide with Phenacylbromide Revisited. Formation of 1,3,4‐Thiadiazines and of Isomeric 1,3‐Thiazoles
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Wolf‐Diethard Pfeiffer Dieter Junghans Ashot S. Saghyan Peter Langer 《Journal of heterocyclic chemistry》2014,51(4):1063-1067
The cyclization of 4‐phenylthiosemicarbazide with phenacylbromide, carried out in refluxing ethanol, afforded 1,3,4‐thiadiazine 1 as the major product. In contrast to a previous report, 2‐phenylimino‐4‐phenyl‐2,3‐dihydro‐1,3‐thiazol‐3‐amine ( 2 ) and not 2‐hydrazono‐3,4‐diphenyl‐2,3‐dihydro‐1,3‐thiazole ( 8 ) was formed as a side‐product. This product is the main product when the reaction is carried out in concentrated hydrochloric acid. Our findings were independently confirmed by independent syntheses of the isomeric products and by a thorough study of their reactivity. It is important to note that the product distribution of the cyclization of thiosemicarbazides with haloketones strongly depends on the substitution pattern and on the reaction conditions. 相似文献
100.
We present results regarding fast and robust solvers for equations arising from continuous and discontinuous Galerkin discretization of heterogeneous diffusion problems in the context of Isogeometric Analysis. The solvers considered belong to the class of non-overlapping domain decomposition methods which use tearing and interconnection strategies. (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献