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Beilstein J. Org. Chem. 2024, 20, 1198–1206, doi:10.3762/bjoc.20.102
Graphical Abstract
Scheme 1: Ring cleavage and ring rearrangement reactions in the biosynthesis of atypical angucyclines.
Figure 1: HPLC traces of reaction mixtures of AlpG, AlpJ, Flu17, and JadG. (a) standards of prejadomycin (9),...
Figure 2: HPLC traces of reactions of JadG, AlpJ, or Flu17 quenched by SOD. (a) 8 + JadG + ʟ-isoleucine; (b) 8...
Scheme 2: Proposed catalytic mechanism of cofactor-independent AlpJ-family oxygenases.
Beilstein J. Org. Chem. 2015, 11, 1089–1095, doi:10.3762/bjoc.11.122
Scheme 1: Synthesis route and chemical structure of the compounds.
Figure 1: Changes in the absorption over time in the UV–vis spectra of dilute THF solution of M0: (a) upon UV...
Figure 2: DSC thermogram of the compounds M0-n obtained on (a) heating and (b) cooling.
Figure 3: Photographic images of the M6 sol-gel transition behavior after UV or visible light irradiation in ...
Figure 4: SEM images of xerogels formed with M6 from solution: (a) ethanol, (b) isopropanol and (c) 1-butanol....
Figure 5: FTIR spectra of gels: (a) powder, (b–d) ethanol, isopropanol and 1-butanol xerogels, respectively.
Figure 6: XRD patterns of xerogels. (a) ethanol, (b) isopropanol and (c) 1-butanol.