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. 2020 Oct 29;142(45):19132–19141. doi: 10.1021/jacs.0c07922

Figure 3.

Figure 3

(a) Design of a C2-symmetric trans-cyclooctene enabling directed tautomerization and enhanced elimination for fast and complete cleavage irrespective of the click orientation. (b) Synthesis of bis-axial and bis-equatorial C2TCO-diol (11) and overlay of schematic 13C NMR spectra of the separated and purified compounds, which indicate C2-symmetry of both isomers resulting from the rigid “crown” (or twist) conformation of the TCO core structure.