| Literature DB >> 17549787 |
Matthew W Powner1, Carole Anastasi, Michael A Crowe, Alastair L Parkes, Jim Raftery, John D Sutherland.
Abstract
Recent work has emphasised the importance of D-ribose aminooxazoline 1 in the synthesis of cytidine ribonucleosides under potentially prebiotic conditions. Upon treatment with cyanoacetylene, 1 is transformed into alpha-D-cytidine (alpha-2), and if an efficient means of anomerising this nucleoside or a derivative thereof were to be found, then the synthesis of one of the key beta-D-nucleosides required to make RNA would be realised. Photoanomerisation of alpha-2 has previously been described, but the yield was extremely low. Therefore, the present study was initiated to determine whether this low yield was the result of a low conversion or competing reaction pathways.Entities:
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Year: 2007 PMID: 17549787 DOI: 10.1002/cbic.200700098
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164