Synthesis of a Stable Hydrophilic trans-Cyclooctene Amino Acid Unlocks Fast Bioorthogonal Click Chemistry for the Generation of Antibody-Drug Conjugates by Genetic Code Expansion.
- DOI
- 10.1002/anie.5717042
- Published
- 2026 Oct 29
- Container
- Angewandte Chemie (International ed. in English)
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1002/anie.5717042,
title = {Synthesis of a Stable Hydrophilic trans-Cyclooctene Amino Acid Unlocks Fast Bioorthogonal Click Chemistry for the Generation of Antibody-Drug Conjugates by Genetic Code Expansion.},
author = {Genov GR and Osmanović D and Bašić I and Koehler C and Sauter PF},
year = {2026},
journal = {Angewandte Chemie (International ed. in English)},
doi = {10.1002/anie.5717042},
url = {https://doi.org/10.1002/anie.5717042}
}RIS
TY - JOUR TI - Synthesis of a Stable Hydrophilic trans-Cyclooctene Amino Acid Unlocks Fast Bioorthogonal Click Chemistry for the Generation of Antibody-Drug Conjugates by Genetic Code Expansion. AU - Genov GR AU - Osmanović D AU - Bašić I AU - Koehler C AU - Sauter PF PY - 2026 JO - Angewandte Chemie (International ed. in English) DO - 10.1002/anie.5717042 UR - https://doi.org/10.1002/anie.5717042 ER -
APA
GR, G., D, O., I, B., C, K., & PF, S. (2026). Synthesis of a Stable Hydrophilic trans-Cyclooctene Amino Acid Unlocks Fast Bioorthogonal Click Chemistry for the Generation of Antibody-Drug Conjugates by Genetic Code Expansion.. Angewandte Chemie (International ed. in English). https://doi.org/10.1002/anie.5717042
Source records
- pubmed · retrieved 2026-11-10T07:14:04.494Z
- europe-pmc · retrieved 2026-11-10T07:14:04.501Z