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Beilstein J. Org. Chem. 2025, 21, 2542–2547, doi:10.3762/bjoc.21.196
Graphical Abstract
Figure 1: Selected natural uracil-containing nucleosides (the key perhydrofuropyran core highlighted in blue)....
Scheme 1: Synthetic strategies toward malayamycin A. (A) Previous synthetic route. (B) Our strategy toward th...
Scheme 2: Rational for intramolecular dipolar cycloaddition.
Scheme 3: Proposed pathway for the enone formation.
Scheme 4: Modified route to access the core of malayamycins.
Scheme 5: Attempting the Baeyer–Villiger reaction.
Beilstein J. Org. Chem. 2024, 20, 3263–3273, doi:10.3762/bjoc.20.270
Figure 1: Fluorotriphenylene derivatives and their nonfluorinated homologs obtained by SNFAr from 2,2'-dilith...
Scheme 1: Synthesis, yields, and nomenclature of 1,2,4-trifluoro-6,7,10,11-tetraalkoxy-3-(perfluorophenyl)tri...
Figure 2: Single crystal structure of 1,2,4-trifluoro-3-(perfluorophenyl)triphenylene (F) viewed along the ma...
Figure 3: POM textures, observed between crossed polarizers of Janus and dimer, F6, F12, G66, and G48, respec...
Figure 4: Comparative bar graph summarizing the thermal behavior of Fn, BTP6, and PHn derivatives (2nd heatin...
Figure 5: Representative S/WAXS patterns of Fn and Gnm compounds.
Figure 6: Absorption (a) and emission (b) spectra of F6 and G66, measured in different solvents at a concentr...
Figure 7: DFT calculated frontier molecular orbitals and optimized molecular structures for F1 and G11.