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All four isomers of substituted 3-alkylthio-4-hydroxybutenes have been synthesised: both the geometry of the double bond and the relative stereochemistry of the two chiral centres are controlled. 相似文献
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N-Acyl derivatives of ,-acosamine and ,-ristosamine were synthesized with high stereo selectivity utilizing intramolecular Michael addition of γ- and δ-carbomoyloxy-α,β-unsaturated esters. 相似文献
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J Leitich 《Tetrahedron letters》1980,21(32):3025-3028
The relative rates of formation of and [2+2]cycloadducts of benzyne to , - and , -1,5-cyclooctadiene, - and -cyclooctene are discussed and properties of the adducts (e.g., their unusual hydrogenation) are described. 相似文献
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1,3,7,9,11,12,14-Heptazapentacene-2,4,8,10 (14,3,9,12)-tetraones (mixed flavins) were prepared by the cyclization of 1,5-dihydro-8-[N-alkyl-N-(5-nitrouracil-6-yl)-amino-5-deazaflavins with Vilsmeier reagent. The mixed flavins oxidized alcohol under neutral condition in sunlight and a remarkable autorecycling was observed. 相似文献
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Methods are described for the stereospecific conversion of hydrindenone 3 either to the corresponding fused or fused hydrindanone (1 or 2, respectively.) 相似文献
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Starting from the coupling reaction of alkyl cuprates with 1-alkynyl-2-propenyl acetates, the title compounds were prepared by short convenient syntheses. 相似文献
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Palladium catalysed alkoxycarbonylation of heterocyclic halides affords a simple and versatile synthesis of both and heterocyclic esters where a range of catalysts have been studied and a method to employ inexpensive inorganic bases has been found. 相似文献
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Toshihiro Hashimoto Motoo Tori Zenei Taira Yoshinori Asakawa 《Tetrahedron letters》1985,26(52):6473-6476
Four novel fusicoccane diterpenoids, fusicoplagins A, B, C, and D, have been isolated from the liverwort subsp. and the structures determined by spectroscopic methods, chemical transformations, and X-ray crystallographic analysis. 相似文献
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Reaction of Ga(CH3)3 with N,N′-dimethyloxamide affords two isomeric N,N′-bis(dimethylgallium)-N,N′-dimethyloxamide complexes, characterized by crystal structure analysis as having cis-and trans-configuration with respect to the central oxamide CC bond and belonging to the point groups C2v (cis) and C2h (trans), respectively. Both isomers which are formed in varying ratio, depending upon the reaction conditions, have been isolated in pure form; their vibration spectra (IR/RE) are analyzed in detail in points of alternative behaviour, and are assigned in all bands, especially in the G-C and Ga-X frequency region. The assignment receives further confirmation from a comparison with the vibrational data of the homologous N,N′-bis(dimethylgallium)oxamide (cis/trans isomer mixture). 相似文献
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The 1H and 13C nmr spectra of , -9-oxobicyclo[3.3.1]nonane-2,4-dicarboxylic acid, 3, in DMSO-d6 or alkaline D2O, clearly show that it exists in a --conformation with carboxyl groups, thus being the first case of - preference of a bicyclo[3.3.1] nonan-9-one due to the presence of ,-2,4- substituents. 相似文献