Nickel-Catalyzed Reductive 1,4-Alkylarylation of 1,3-Enynes with Aziridines and Aryl Electrophiles: A Route to γ-Sulfonamide Allenes
- DOI
- 10.1021/acs.orglett.6c02492
- Published
- 2026-07-29
- Container
- Organic Letters
- Publisher
- American Chemical Society (ACS)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/acs.orglett.6c02492,
title = {Nickel-Catalyzed
Reductive 1,4-Alkylarylation of 1,3-Enynes
with Aziridines and Aryl Electrophiles: A Route to γ-Sulfonamide
Allenes},
author = {Feng Zhang and Jing-Wen Shao and Ting-Jin Li and Jianing Xie and Yan Li},
year = {2026},
journal = {Organic Letters},
doi = {10.1021/acs.orglett.6c02492},
url = {https://doi.org/10.1021/acs.orglett.6c02492}
}RIS
TY - JOUR TI - Nickel-Catalyzed Reductive 1,4-Alkylarylation of 1,3-Enynes with Aziridines and Aryl Electrophiles: A Route to γ-Sulfonamide Allenes AU - Feng Zhang AU - Jing-Wen Shao AU - Ting-Jin Li AU - Jianing Xie AU - Yan Li PY - 2026 JO - Organic Letters DO - 10.1021/acs.orglett.6c02492 UR - https://doi.org/10.1021/acs.orglett.6c02492 ER -
APA
Zhang, F., Shao, J., Li, T., Xie, J., & Li, Y. (2026). Nickel-Catalyzed Reductive 1,4-Alkylarylation of 1,3-Enynes with Aziridines and Aryl Electrophiles: A Route to γ-Sulfonamide Allenes. Organic Letters. https://doi.org/10.1021/acs.orglett.6c02492
Source records
- crossref · retrieved 2026-09-25T11:44:15.335Z