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THE STEREOCHEMICAL CONFIGURATIONS OF THE SUGARS FUCOSE AND RHODEOSE. 2

✍ Scribed by Hudson, C. S.

Book ID
127012274
Publisher
American Chemical Society
Year
1911
Tongue
English
Weight
401 KB
Volume
33
Category
Article
ISSN
0002-7863

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πŸ“œ SIMILAR VOLUMES

Stereochemical studies on esperamicins:
Stereochemical studies on esperamicins: Determination of the absolute configuration of hydroxyamino sugar fragment.
✍ J. Golik; H. Wong; B. Krishnan; D.M. Vyas; T.W. Doyle πŸ“‚ Article πŸ“… 1991 πŸ› Elsevier Science 🌐 French βš– 219 KB

The 0-D-gluco-hexopyranose configuration has been assigned for the hydroxyamino sugar fragment of esperamicin A'. This determination concluded our study on the absolute configuration of the carbohydrate portion of esperamicins. Since our first report on the structure elucidation of esperamicins A,,

Stereochemical studies on esperamicins:
Stereochemical studies on esperamicins: Determination of the absolute configuration of isopropylamino sugar moiety
✍ J. Golik; H. Wong; D.M. Vyas; T.W. Doyle πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 201 KB

The absolute stereochmistry of the isopropylamino sugar moiety of esperamicin A1 was determined as the g-&-threo-pentopyranosyl by comparing the CD spectra of derivatized methanolysis product 4 with those of two synthesized antipodal glycosides 2 and Is.