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排序方式: 共有385条查询结果,搜索用时 31 毫秒
1.
W. Fleischhacker K. Florkova B. Richter 《Monatshefte für Chemie / Chemical Monthly》1994,125(3):345-353
Summary Following our concept of rather new structural variations in the nitrogen region of morphine alkaloids we describe the first synthesis of N/C-10-bridged tertiary bases. 相似文献
2.
D iels-A lder反应具有立体专一性和很好的区域选择性,已被大量应用于天然有机化合物、香料、药物等的合成中。一般说来,D iels-A lder反应在加热条件下即能发生,但加热往往导致反应的区域选择性和立体专一性下降,而研究表明,路易斯酸催化下的D iels-A lder反应在不同程度上表现出或反应速度加快,或产率提高,或条件温和,尤其是区域选择性和立体专一性得到提高等良好特性。呋喃类化合物由于呋喃环所具有的芳香性而较难与一般的亲双烯发生D iels-A lder反应。如呋喃和丙烯酸甲酯在加热条件下反应2~3个月,产率只能达到50%,且反应温度的提高… 相似文献
3.
N. S. Arutyunyan L. A. Akopyan G. A. Gevorgyan G. M. Snkhchyan G. A. Panosyan 《Chemistry of Heterocyclic Compounds》2005,41(4):437-441
A preparative method was developed for the synthesis of ethyl furfurylidenecyanoacetate. Its condensation with phenylmagnesium bromide gave ethyl α-cyano-β-(2-furyl)hydrocinnamate, the decarboxylation of which led to β-(2-furyl)hydrocinnamonitrile. Reduction of this nitrile with lithium aluminum hydride gave 2-(3-amino-1-phenylpropyl)furan. Some of its transformations were studied.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 517–521, April, 2005. 相似文献
4.
AbstractA convergent synthesis of the southern furan segment of novel furanocembranoids from Croton oblongifolius has been accomplished involving silver-catalyzed cyclization of alkynyl diol as the key step towards 2, 5-disubstituted furan ring formation. 相似文献
5.
利用Mn^2+,Ba^2+及Sr^2+作为模板离子,合成了一类新型的含呋喃环系 Schiff碱型大环化合物,如L^1和配合物L^2Ba(ClO4)2,L^3Ba(ClO4)2和L^4Ba (ClO4)2.L^2-L^4的Ba^2+配合物经与NaSO4水溶液反应解络,得到自由配体L^2, L^3和L^4,配体L^2和L^3分别与Sr^2+作用,得到配合物L^2Sr(ClO4)2和L^3Sr (ClO4)2。上述大环配体和各种配合物均经元素分析,IR,^1H NMR,MS等证实了它 们的结构和组成。 相似文献
6.
Density functional theory and ab initio calculations have been used to determine structures and stabilities of the protonated aromatics species AH^+ and AH2^2+ (A=pyrrole, furan). Possible mechanisms and relative energetics for protonation of pyrrole and furan by H3O^+ and AH^+ in the gas phase have been explored. Calculations show that the Cα-protonated species was the most stable structure for AH^+, and the protonated AH^+ might accommodate the second proton to yield AH2^2+ if the free proton was available. The gas-phase H3O^+ could protonate pyrrole and furan with significant exothermiCity and almost without barrier. The proton transfer from AH4^+ to pyrrole and furan has a barrier ranging from 33.5 to 39.3 kJ/mol in the gas phase. 相似文献
7.
《Tetrahedron》2003,59(16):2801-2809
A series of furan C-nucleosides having a sulfur atom in the sugar ring were synthesised. The α and β anomers of 3-ethoxycarbonyl-2-methyl-5-(4′-thio-d-erythrofuranosyl)furans 10 and 11 were obtained by acid treatment of (4′-S-acetyl-4′-thio-d-arabino-tetritol-1-yl)furan 9. Oxidation of 10 with m-chloroperbenzoic acid gave sulfoxide 12 as one epimer at the sulfur atom whereas 11 was transformed into sulfoxide 13 as an epimeric mixture. S-Methylation of 10 and 11 with methyl triflate led to sulfonium salts 14 and 15. The prepared compounds were found to be moderate inhibitors of α-l-fucosidase. 相似文献
8.
Krayushkin M. M. Ivanov S. N. Martynkin A. Yu. Lichitsky B. V. Dudinov A. A. Uzhinov B. M. 《Russian Chemical Bulletin》2001,50(12):2424-2427
Procedures were developed for the synthesis of substituted bis(2,5-dimethyl-3-thienyl)furans based on 1,2-bis(2,5-dimethyl-3-thienyl)-2-hydroxyethanone. Dithienylethene structures in which the ethene fragment is involved in the furan or furopyrimidine system possess photochromic properties and their open forms exhibit fluorescence. 相似文献
9.
Acylation of substituted 4-(furyl-2)-4-arylaminobut-1-enes with maleic anhydride provided 2-allyl-6-carboxy-4-oxo-3-aza-10-oxatricyclo[5.2.1.01,5]dec-8-enes in high yield under mild reaction conditions. The Diels-Alder adducts are formed via an initial amide formation followed by a stereoselective intramolecular [4+2] exo-cycloaddition reaction. Treatment of the tricyclic compounds with phosphoric acid at high temperatures (70-120 °C) promoted cyclic ether opening, intramolecular cyclization and aromatization to give the corresponding tetracyclic compounds, 5,6,6a,11-tetrahydro-10-carboxyisoindolo[2,1-a]quinolines, in moderate yields. The influence of the acid and the reaction temperature on the cyclization reactions are also discussed. 相似文献
10.
An innovative route for the synthesis of substituted naphtho[2,1-b]furan has been delineated through a ring transformation reaction of suitably functionalized 2H-pyran-2-ones by reaction with 6,7-dihydro-5H-benzofuran-4-one, in good yield. 相似文献