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. 2026 Feb 20;18(5):893–898. doi: 10.1038/s41557-026-02077-x

Table 2.

Substrate scope of bioactive molecules and dienophiles

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aAcid (2 equiv.), maleimide-fluorescein (1 equiv.) was added. bReaction conditions: HFIP (0.1 ml), xylene (1.0 ml), 4.0 equiv. LiCl, 160 °C, 18 h. cReaction conditions: HFIP (0.5 ml), xylene (0.5 ml), 2.0 equiv. NaH2PO4, 150 °C, 18 h. dReaction conditions: HFIP (0.5 ml), xylene (0.5 ml), 150 °C, 18 h. eReaction conditions: HFIP (0.5 ml), xylene (0.5 ml), 1.0 equiv. KH2PO4, acid 5 equiv., vinylphenylketone 1 equiv., 160 °C, 18 h. fReaction conditions: HFIP (0.5 ml), xylene (0.5 ml), acid 5 equiv., methyl acrylate 1 equiv., Pd(OAc)2 were used as catalysts, 160 °C, 18 h.