Stereostructure assignment of flexible five-membered rings by GIAO 13C NMR calculations: prediction of the stereochemistry of elatenyne.
The stereochemistry of conformationally mobile five-membered rings is often hard to assign from NMR data, and [2,2']bifuranyl systems are even more challenging. GIAO (13)C NMR chemical shifts have been calculated for a series of [2,2']bifuranyl and pyranopyran species, taking into account...
المؤلفون الرئيسيون: | Smith, S, Paton, R, Burton, J, Goodman, J |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2008
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مواد مشابهة
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Studies on the synthesis of elatenyne.
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Total synthesis and structure confirmation of elatenyne: success of computational methods for NMR prediction with highly flexible diastereomers.
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Synthesis and stereochemistry of 6-membered ring phosphonates
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Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula.
حسب: Sheldrake, H, وآخرون
منشور في: (2009) -
Expanding the Utility of Bioinformatic Data for the Full Stereostructural Assignments of Marinolides A and B, 24- and 26-Membered Macrolactones Produced by a Chemically Exceptional Marine-Derived Bacterium
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منشور في: (2023-06-01)