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101.
We describe a route for the polymer supported total synthesis of the cyclic bisbibenzyls of the isoplagiochin type found in liverworts. TentaGel® resins were used as solid support for a sequence involving Suzuki, Wittig and hydrogenation protocols. The polymer linked intermediates could be characterized by HR-MAS NMR. This route is to be extended to the synthesis of small libraries of differently halogenated derivatives. 相似文献
102.
The first isocyanide ligated hexanuclear zirconium halide cluster is reported. The unoxidized [(Zr6Be)Cl12(CNXyl)6] (CNXyl = 2,6-dimethylphenyl isocyanide) was obtained from the solid state precursor K3Zr6Cl15Be by dissolution in CH3CN in the presence of CNXyl. The CNXyl ligands occupy all the axial positions on the cluster. The compound was recrystallized from CH2Cl2 and Et2O. [(Zr6Be)Cl12(CNXyl)6].2CH2Cl2 crystallizes in the space group
(#2) with a = 12.092(5) Å, b=12.728(5) Å, c = 14.102(8) Å, = 104.98(4)°, =107.11°, = 100.94°, V = 1919(2) Å3, Z = l, R = 11.3% and R
W
= 27.0%. For the bound isocyanide ligands, v
CN increases to 2140 cm–1. 相似文献
103.
α-Bromo benzolymethylene triphenylphosphorane 3 has been synthesized by the reaction of benzoylmethylene triphenylphosphorane 1 with N-bromosuccinimide in the yield of 87% and can react with aromatic aldehydes 4 to give α-bromochalcones 5 in good yields. 相似文献
104.
105.
Twenty-one new organogermanium compounds with the formulae Ph3GeCHR1CH2CONHNHC(X)NHR2 (1) (R1=H, Ph; = Ph, p-CH3Ph, O -CH3Ph, p-ClPh, COPh, X = S, O) and (R1 = H, Ph; R2 = Ph, p-CH3Ph, o-CH3Ph, p-ClPh; X=S, O) were synthesized and characterized by elemental analysis, 1H NMR, IR, MS and X-ray diffraction techniques. Compounds l were prepared by the reactions of Ph3GeCHR1CH2CONHNH2 with R2NCX in chloroform in 77-94% yields, and 2 were obtained by refluxing l with sodium hydroxide (8%) with yields of 55-94%. 相似文献
106.
107.
Christian R. Noe M. Knollmüller G. Steinbauer E. Wagner H. Kürner P. Ettmayer H. Völlenkle 《Monatshefte für Chemie / Chemical Monthly》1991,122(4):299-317
Summary Enantiomerically pure 1,2-diols bearing optionallysyn oranti configurated secondary hydroxylic groups are synthesized from acetal-protected cyanohydrins. After resolution of the diastereomers the cyanohydrins are converted into -alkoxy-ketones by Grignard-reaction followed by reduction using common chelating or non-chelating agents. Among others syntheses of enantiomerically pure pheromones,endo-Brevicomin,exo-Brevicomin and Dispalure are given as examples.
Prof. Dr. Hans Berbalk zum 70. Geburtstag gewidmet 相似文献
108.
U. M. Dzhemilev A. G. Ibragimov A. B. Morozov R. R. Muslukhov G. A. Tolstikov 《Russian Chemical Bulletin》1992,41(6):1089-1093
A new stereoselective method is developed for the synthesis of 1-chloro-, 1-alkoxy-, and 1-N,N-dialkylaminoalumino-cyclopentanes from -olefins, metallic magnesium, and aluminum halides (AlCl3, RO-AlCl2, R2N-AlCl2) in the presence of catalytic amounts of Cp2ZrCl2 (Cp=5-C5H5). The products from hydrolysis and deuterolysis of the Al-substituted 3,4-dialkylaluminocyclopentanes (ACP) have the threo configuration.For Communication 8, see [1].Institute of Organic Chemistry, Urals Branch, Russian Academy of Sciences, 450054 Ufa. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 6, pp. 1393–1397, June, 1992. 相似文献
109.
Yu. N. Belokon' 《Russian Chemical Bulletin》1992,41(5):868-884
The complexes of glycine, -alanine, and -alanine with (S)-[N-(N-benzylprolyl)amino] benzophenone formed by Ni(II) and Cu(II) ions and Schiff bases enter into different nucleophilic and electrophilic reactions with the formation of diastereoisomeric complexes which decompose into proteinogenic and nonproteinogenic L-amino acids with a high chemical yield and elevated optical purity (70–90%). Optically pure amino acids can be obtained from diastereoisomerically pure complexes after the complexes are separated by recrystallization of the mixture of diastereoisomeric complexes formed. A new type of interphase catalysts of C-alkylation of achiral Schiff bases was proposed. The catalysts are positively charged Ni(II) and Cu(II) complexes of Schiff bases of chiral diamines. In some cases, these complexes have a higher activity and capacity to execute asymmetric alkylation than traditional chiral interphase catalysts based on cinchonidine.Based on materials in the section report by Yu. N. Belokon' to the 7th European Symposium on Organic Chemistry, ESOC-7.A. N. Nesmeyanov Institute of Organoelemental Compounds, Russian Academy of Sciences, 117813 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 5, pp. 1106–1127, May, 1992. 相似文献
110.
Nous quantifions certaines inclusions d'algèbres de Lie semi-simpleshg. Nous calculons les homologies associées aux quantifications, surC((h)), d'une part des algèbres de fonctions formelles surG/H, pourHG une inclusion de groupes de Lie semi-simples associée, et d'autre part des fonctions algébriques sur SL(2,C)/T.We quantize certain inclusions of semisimple Lie algebrashg. We compute the cyclic and Hochschild homologies for theC((h))-quantizations of
相似文献
(1) | the ring of formal functions onG/H,G andH semisimple Lie groups associated to these inclusions, and |
(2) | the ring of algebraic functionsSL(2,C)/T (T being the nonquantized torus of SL(2, C)). |