Gerald Richter

Find an error

Name:
Organization: Cardiff University
Department: School of Chemistry, Main Building
Title:
Co-reporter:Andrew C. Wood, David W. Knight, Gerald Richter
Tetrahedron 2015 Volume 71(Issue 11) pp:1679-1683
Publication Date(Web):18 March 2015
DOI:10.1016/j.tet.2015.01.053
The cofactor forms of riboflavin (FMN and FAD) play a crucial role in the mediation of both enzymatic processes and light perception by photo-sensitive proteins, and thus structural analogues of this chromophore are highly useful tools to assist in the elucidation of enzymatic mechanisms. 1-Deazariboflavin has been rarely utilised for this purpose, due in part to its previously difficult and inefficient synthesis. Recent examination has enabled a remarkable improvement in the overall synthetic yield from 11.0 to 61.3%, allowing reliable production of 1-deazariboflavin for use as a tool in enzymatic mechanistic determination.
D-RIBITOL, 1-[(2-AMINO-4,5-DIMETHYLPHENYL)AMINO]-1-DEOXY-
D-Ribitol,1-deoxy-1-(2,3-dihydro-7,8-dimethyl-1,3-dioxopyrido[3,4-b]quinoxalin-5(1H)-yl)-
Pentanedioic acid, 2-bromo-3-oxo-, diethyl ester
Piperidine-2,4,6-trione