Controlled reactive intermediates enabling facile molecular conjugation

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Abstract

Reliable methods to conjugate molecules using highly reactive substrates including strained cycloalkynes, azides, and thiophene S, S-dioxides, or short-lived intermediates such as arynes and 6- and 7-membered cycloalkynes have been developed. This account describes our recent achievement on the development of facile methods conjugating a wide variety of molecules based on the reactivity of controlled short-lived intermediates.

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Yoshida, S. (2018). Controlled reactive intermediates enabling facile molecular conjugation. Bulletin of the Chemical Society of Japan, 91(8), 1293–1318. https://doi.org/10.1246/bcsj.20180104

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