H NMR conformational analysis of acylated glycerolyl flavazoles
Joint Authors
Masud, Ahmad
Awad, Layla
al-Kilani, Yeldez
al-Ashri, al-Sayyid H.
Source
The Arabian Journal for Science and Engineering
Issue
Vol. 15, Issue 1 (31 Jan. 1990), pp.105-110, 6 p.
Publisher
King Fahd University of Petroleum and Minerals
Publication Date
1990-01-31
Country of Publication
Saudi Arabia
No. of Pages
6
Main Subjects
Topics
Abstract EN
The conformation of l-aryl-3-(D-erythro-1, 2, 3-triacetoxypropyl)-6, 7-dimethyl-flavazoles and their L-threo analogs have been examined by 1H NMR spectroscopy.
The favored conformation can be deduced from the spin-spin coupling data.
The most popular conformation of the D-erythro analogs is the extended zigzag conformations, whereas the sickle conformation of the L-threo analogs is the most popular one.
However, a bent conformation is the most popular for the benzoyloxy analogs of the D-erythro isomers.
American Psychological Association (APA)
Masud, Ahmad& Awad, Layla& al-Kilani, Yeldez& al-Ashri, al-Sayyid H.. 1990. H NMR conformational analysis of acylated glycerolyl flavazoles. The Arabian Journal for Science and Engineering،Vol. 15, no. 1, pp.105-110.
https://search.emarefa.net/detail/BIM-570995
Modern Language Association (MLA)
Masud, Ahmad…[et al.]. H NMR conformational analysis of acylated glycerolyl flavazoles. The Arabian Journal for Science and Engineering Vol. 15, no. 1 (Jan. 1990), pp.105-110.
https://search.emarefa.net/detail/BIM-570995
American Medical Association (AMA)
Masud, Ahmad& Awad, Layla& al-Kilani, Yeldez& al-Ashri, al-Sayyid H.. H NMR conformational analysis of acylated glycerolyl flavazoles. The Arabian Journal for Science and Engineering. 1990. Vol. 15, no. 1, pp.105-110.
https://search.emarefa.net/detail/BIM-570995
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 109-110
Record ID
BIM-570995
