An NMR and ab initio MO study of the effect of β-oxygen in 1,3-dioxanes
Abstract
NMR Measurements and ab initio calculations suggest that in 1,3-dioxanes the β-oxygen atoms have the effect of weakening the equatorial CH bond at the 5-position.
NMR Measurements and ab initio calculations suggest that in 1,3-dioxanes the β-oxygen atoms have the effect of weakening the equatorial CH bond at the 5-position.
Please wait while we load your content...
Something went wrong. Try again?
J. E. Anderson, A. J. Bloodworth, J. Cai, A. G. Davies and C. H. Schiesser, J. Chem. Soc., Perkin Trans. 2, 1993, 601 DOI: 10.1039/P29930000601
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Fetching data from CrossRef.
This may take some time to load.
Loading related content