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Titlebook: Carbohydrates; Synthesis, Mechanism Momcilo Miljkovic Book 2009 Springer-Verlag New York 2009 Carbohydrate.Chemistry.Glycoscience.Miljkovic

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樓主: 弄碎
31#
發(fā)表于 2025-3-27 00:50:39 | 只看該作者
On MV-algebras of continuous functionsmotion, vibrating and rotating about chemical bonds. The deformation of chemical bonds due to vibration (stretching, wagging, etc.) of atoms is quantized and it is not the subject of conformational analysis. However, the rotation of atoms about the single bonds is the subject of conformational analysis.
32#
發(fā)表于 2025-3-27 02:22:39 | 只看該作者
33#
發(fā)表于 2025-3-27 06:37:45 | 只看該作者
34#
發(fā)表于 2025-3-27 11:55:57 | 只看該作者
35#
發(fā)表于 2025-3-27 17:05:11 | 只看該作者
Masaki Kashiwara,Michèle Vergnes of macrolide antibiotics represents one such difficult problem. They consist of macrocyclic lactone rings with many hydroxylated and methylated chiral carbons. In addition to that the macrocyclic lactones (macrolides) are usually glycosylated with amino sugars.
36#
發(fā)表于 2025-3-27 19:25:34 | 只看該作者
Chemistry of the Glycosidic Bond, and phosphatidyl inositol. The glycosidic bond can also be formed between the anomeric C1 carbon of a monosaccharide and the amido nitrogen of asparagine (as, for example, in N-linked glycoproteins) or the nitrogen of a purine or a pyrimidine base (as, for example, in ribo- and deoxyribonucleosides
37#
發(fā)表于 2025-3-27 22:28:19 | 只看該作者
Non-commutative Algebraic Geometry and phosphatidyl inositol. The glycosidic bond can also be formed between the anomeric C1 carbon of a monosaccharide and the amido nitrogen of asparagine (as, for example, in N-linked glycoproteins) or the nitrogen of a purine or a pyrimidine base (as, for example, in ribo- and deoxyribonucleosides
38#
發(fā)表于 2025-3-28 05:37:54 | 只看該作者
39#
發(fā)表于 2025-3-28 08:08:33 | 只看該作者
40#
發(fā)表于 2025-3-28 12:54:51 | 只看該作者
Ulrich H?hle,Erich Peter Klements, the conformational mixture of cyclohexanol or its methyl ether contains, at equilibrium, 89% of the conformer with equatorially oriented hydroxyl or methoxy group and 11% of the conformer with axially oriented hydroxyl or methoxy group, indicating clear preference for the equatorial conformer (Fig. 3.1).
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