Selective nucleophilic addition of aryllithium reagents to α-ketonitriles giving ketones under microflow conditions.

Qenawy MS, Okamoto K, Nagaki A

DOI: 10.1039/d5cc07035j
Published: 2026 Apr 2
Container: Chemical communications (Cambridge, England)
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1039/d5cc07035j,
  title = {Selective nucleophilic addition of aryllithium reagents to α-ketonitriles giving ketones under microflow conditions.},
  author = {Qenawy MS and Okamoto K and Nagaki A},
  year = {2026},
  journal = {Chemical communications (Cambridge, England)},
  doi = {10.1039/d5cc07035j},
  url = {https://doi.org/10.1039/d5cc07035j}
}

RIS

TY  - JOUR
TI  - Selective nucleophilic addition of aryllithium reagents to α-ketonitriles giving ketones under microflow conditions.
AU  - Qenawy MS
AU  - Okamoto K
AU  - Nagaki A
PY  - 2026
JO  - Chemical communications (Cambridge, England)
DO  - 10.1039/d5cc07035j
UR  - https://doi.org/10.1039/d5cc07035j
ER  -

APA

MS, Q., K, O., & A, N. (2026). Selective nucleophilic addition of aryllithium reagents to α-ketonitriles giving ketones under microflow conditions.. Chemical communications (Cambridge, England). https://doi.org/10.1039/d5cc07035j

Source records

pubmed · retrieved 2026-11-10T08:51:49.717Z