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- 01H6XKYBA8KV5TF1EFS9199D8C classification A1.
- 01H6XKYBA8KV5TF1EFS9199D8C date "1977".
- 01H6XKYBA8KV5TF1EFS9199D8C language "eng".
- 01H6XKYBA8KV5TF1EFS9199D8C type journalArticle.
- 01H6XKYBA8KV5TF1EFS9199D8C hasPart 01H6XMDQE41K05DKZD1WN9KAES.pdf.
- 01H6XKYBA8KV5TF1EFS9199D8C subject "Chemistry".
- 01H6XKYBA8KV5TF1EFS9199D8C doi "10.1135/cccc19773057".
- 01H6XKYBA8KV5TF1EFS9199D8C issn "0010-0765".
- 01H6XKYBA8KV5TF1EFS9199D8C issn "1212-6950".
- 01H6XKYBA8KV5TF1EFS9199D8C issue "10".
- 01H6XKYBA8KV5TF1EFS9199D8C volume "42".
- 01H6XKYBA8KV5TF1EFS9199D8C abstract "Through the determination of the chemical shift increments for the ring protons in pyranoses at the geminal and vicinal positions of a methoxy grouping it is possible to obtain qualitative insight about the rotameric states of the latter. This is exemplified on methyl α- and β-D-glucopyranoside, 2-O-methyl-α- and -β-D-glucopyranose, 3-O-methyl-β-D-gulopyranose, 4-O-methyl-α- and β-L-arabinopyranose and methyl 2-O-methyl-α- and -β-glucopyranoside. It is stated that an H-5 axial proton is much less deshielded by an axial methyxo group at the anomeric position than by the hydroxyl function. a small shielding for protons involved in H(g+, g-,g-)CH3 or H(g-,g+,a)CH3 conformational fragments (δ-effect) seems to occur.".
- 01H6XKYBA8KV5TF1EFS9199D8C author 6D9E4C9A-B25E-11E6-B104-2D2FD0AF0289.
- 01H6XKYBA8KV5TF1EFS9199D8C author 739A5486-B25E-11E6-B104-2D2FD0AF0289.
- 01H6XKYBA8KV5TF1EFS9199D8C author urn:uuid:f1bebdc4-f52d-4d16-a6d8-f57ecc5253cd.
- 01H6XKYBA8KV5TF1EFS9199D8C dateCreated "2023-08-03T11:53:47Z".
- 01H6XKYBA8KV5TF1EFS9199D8C dateModified "2024-10-29T17:44:55Z".
- 01H6XKYBA8KV5TF1EFS9199D8C name "Rotameric behaviour of methoxy groups in some aldopyranoses".
- 01H6XKYBA8KV5TF1EFS9199D8C pagination urn:uuid:cdc5db5d-717d-49e0-88a9-5d23f103bbe7.
- 01H6XKYBA8KV5TF1EFS9199D8C sameAs LU-01H6XKYBA8KV5TF1EFS9199D8C.
- 01H6XKYBA8KV5TF1EFS9199D8C sourceOrganization urn:uuid:9a9e8769-56bb-40f0-bea2-6f7d7873b4f7.
- 01H6XKYBA8KV5TF1EFS9199D8C type A1.