Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The synthesis of uracil/thymine containing tetra/trisubstituted imidazole derivatives was demonstrated using Ugi/Passerini-reaction followed by a postcyclization reaction sequence. The approach enables the one-pot facile construction of diverse compounds in moderate to excellent yields (47-82%). The 5-fluorouracil and 5-methyluracil moieties afford potentially bioactive molecules with drug-like properties. These scaffolds are currently being utilized in the screening deck of the European Lead Factory.

More information Original publication

DOI

10.1021/acscombsci.7b00145

Type

Journal article

Publication Date

2018-04-09T00:00:00+00:00

Volume

20

Pages

192 - 196

Total pages

4

Keywords

Passerini-3CR, Ugi-4CR, imidazole, one-pot, uracil/thymine, Cyclization, Humans, Hydrogen Bonding, Imidazoles, Magnetic Resonance Spectroscopy, Models, Molecular, Molecular Structure, Small Molecule Libraries, Thymine, Uracil