The δ rather than the γ-lactone structure is proposed for dehydro-L-ascorbic acid phenylosazone. This is supported by its failure to react with periodate and by its i.r. and n.m.r. spectra. Acetates and benzoates of dehydro-L-ascorbic acid arylosazones are described.
H. E. Khadem and S. H. E. Ashry, J. Chem. Soc. C, 1968, 2247 DOI: 10.1039/J39680002247
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.
Please wait while we load your content...