Monoselective Mechanochemical Aromatic Nucleophilic Substitution Enabled by Crystal-Engineering-Guided Reaction Design.
- DOI
- 10.1002/anie.2656827
- Published
- 2026 Jun 8
- Container
- Angewandte Chemie (International ed. in English)
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/anie.2656827,
title = {Monoselective Mechanochemical Aromatic Nucleophilic Substitution Enabled by Crystal-Engineering-Guided Reaction Design.},
author = {Kawamura S and Yamamoto H and Jin M and Kubota K and Ito H},
year = {2026},
journal = {Angewandte Chemie (International ed. in English)},
doi = {10.1002/anie.2656827},
url = {https://doi.org/10.1002/anie.2656827}
}RIS
TY - JOUR TI - Monoselective Mechanochemical Aromatic Nucleophilic Substitution Enabled by Crystal-Engineering-Guided Reaction Design. AU - Kawamura S AU - Yamamoto H AU - Jin M AU - Kubota K AU - Ito H PY - 2026 JO - Angewandte Chemie (International ed. in English) DO - 10.1002/anie.2656827 UR - https://doi.org/10.1002/anie.2656827 ER -
APA
S, K., H, Y., M, J., K, K., & H, I. (2026). Monoselective Mechanochemical Aromatic Nucleophilic Substitution Enabled by Crystal-Engineering-Guided Reaction Design.. Angewandte Chemie (International ed. in English). https://doi.org/10.1002/anie.2656827
Source records
- pubmed · retrieved 2026-09-24T21:20:48.818Z