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- W2080296075 endingPage "7326" @default.
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- W2080296075 abstract "The unsaturated ester aldehyde, (E)-3-alkoxycarbonyl-5-phenyl-2,4-dienal, was efficiently dimerized by applying the strain-promoted double-click reaction with sym-dibenzo-1,5-cyclooctadiene-3,7-diyne. The resulting dimerized probe was sequentially reacted first with one peptide molecule and then with a protein or the amino groups on the surface of a live cell through double azaelectrocyclization to achieve highly efficient bioconjugation." @default.
- W2080296075 created "2016-06-24" @default.
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- W2080296075 date "2013-01-01" @default.
- W2080296075 modified "2023-09-24" @default.
- W2080296075 title "Development of bis-unsaturated ester aldehydes as amino-glue probes: sequential double azaelectrocyclization as a promising strategy for bioconjugation" @default.
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- W2080296075 doi "https://doi.org/10.1039/c3ob41507d" @default.
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