Stereoelectronic and conformational effects on the stereochemical course of reduction of bicyclo[3.3.1]nonane 1,3-diketones

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作者：

机构：

[1] Butkus, Eugenius

[2] Stončius, Arvydas

[3] Malinauskiene, Jule

[4] Tomoda, Shuji

[5] Kaneno, Daisuke

来源：

Butkus, E. (eugenijus.butkus@chf.vu.lt) | 2001年 / National Research Council of Canada卷 / 79期

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D O I：

10.1139/v01-131

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[41] POLAROGRAPHIC REDUCTION OF COPPER CHELATES OF 1,3-DIKETONES .4. CHELATE STABILITY AND ELECTRON-TRANSFER MECHANISM
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[47] Stereoelectronic effects on the conformational properties of 1,3-dioxane, 1,3-dithiane, and 1,3-diselenane: An ab initio study and NBO analysis
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[49] TiCl4-mediated reduction of 1,3-diketones with BH3-pyridine complex:: A highly diastereoselective method for the synthesis of syn-1,3-diols
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[50] STEREOCHEMICAL AND C-13 NMR SPECTROSCOPICAL INVESTIGATIONS .25. CONFORMATIONAL RELAXATION AS LIMITATION OF CHEMICAL-MODELS - EMPIRICAL FORCE-FIELD CALCULATIONS AND C-13 NMR SHIELDING EFFECTS FOR SOME CYCLOHEXANES, BICYCLO[2.2.1]HEPTANES, BICYCLO[3.3.1]NONANE, AND 11 BETA-SUBSTITUTED ESTRENES
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