Concise Synthesis of the Click-to-Release Linker iTCO Enabled by Telescoped Flow Photohydrolysis and Iodolactonization
The tetrazine-trans-cyclooctene (Tz-TCO) click-to-release reaction is widely used for bioorthogonal payload release in chemical biology and drug delivery. The recently developed intramolecularly controlled click-cleavable trans-cyclooctene linker iTCO enables fast, near-quantitative release across diverse tetrazine classes, but its broader use has been limited by a lengthy, low-yielding synthesis (eleven steps, ∼1% overall yield). We report a seven-step route centered on a telescoped flow photohydrolysis-iodolactonization sequence, providing gram-scale access to iTCO in 8% overall yield.
Authors
- Andreas Löffler (ORCID: https://orcid.org/0000-0001-6910-6813)
- Hannes Mikula (ORCID: https://orcid.org/0000-0002-9218-9722)
- Johannes Bintinger (ORCID: https://orcid.org/0000-0002-6397-4254)
- Sebastian Hecko (ORCID: https://orcid.org/0000-0002-6210-4425)
- Sebastian Schnöll (ORCID: https://orcid.org/0009-0007-5164-3232)
- Jakob Raffler (ORCID: https://orcid.org/0009-0008-5556-7078)
Institutions
- TU Wien (AT)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-11-05
- DOI
- https://doi.org/10.1021/acs.joc.6c02268
- Primary Topic
- Click Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00