Prolonged illumination of 8-X-5-deazaflavins (X = NH2 or NMe2) in the presence of triethanolamine as electron donor leads to the formation of 6,7-dihydro-8-X-5-deazaflavins, while using ethylenediaminetetra-acetate or oxalate as electron donor, besides the 6,7-dihydro compound the dimeric product 5,5′-bis(1,5-dihydro-3-carboxymethyl-8-X-5-deazaflavin) is formed.
P. A. J. Link, H. C. van der Plas and F. Müller, J. Chem. Soc., Chem. Commun., 1986, 1385 DOI: 10.1039/C39860001385
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...