共查询到20条相似文献,搜索用时 15 毫秒
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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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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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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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Rhodium(III)tetraphenylporphyrin behaves as a sterically hindered cyclopropanation catalyst. Cis-cyclopropanes or “abnormal” products are obtained on reaction with cis-olefins or aromatics. 相似文献
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A novel olefin metathesis sequence permits ready access to functionalised , , -tricyclo [6.3.0.02,6] undecane based bis-enones. These bis-enones have been shown to undergo cage cyclisation in sunlight with remarkable ease and efficiency. 相似文献
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Intramolecular DIELS-ALDER reactions of requisite trienes led to -1-decalones, an endo intermediate state. 相似文献
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Claudio Fuganti Piero Grasselli Stefano Servi Carlo Zirotti 《Tetrahedron letters》1982,23(41):4269-4272
The C4erythro and threo diols (7) and (8) are converted either into the chiral epoxides (13) and (15) or into the enantiomers (14) and (16); the epoxide (13) is used as chiral synthon for the preparation of (3,4) 4-methyl-3-heptanol (21). 相似文献
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Michael J. Cook Michael H. Abraham Luigi E. Xodo Raymond Cruz 《Tetrahedron letters》1981,22(31):2991-2994
Head space analysis, GLC retention time data, and solution calorimetry are used to determine the effect of medium on the thermodynamic parameters for the equilibrium (1) ? (2). It is shown that changes in ΔG° and ΔH° can be evaluated for the transfer of the equilibrium from a series of solvents to the gaseous phase which is used as the reference medium. 相似文献
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The 6-hydroperoxy-1,4-cyclooctadiene (), which is formed in the photosensitized oxygenation of 1,5-cyclooctadiene (), affords on further singlet oxygenation 5,8-dihydroperoxy-1,3-cyclooctadiene (), which via triphenylphosphine reduction leads to -5,8-dihydroxy-1,3-cyclooctadiene () and subsequent pyridinium chlorochromate oxidation to 1,3-cyclooctadien-5,8-dione (). 相似文献
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