Intermolecular defluorinative 1,2-diamination of fluoroalkenyl iodides with sulfonamides: synthesis of acyclic and cyclic fluorinated 1,2-enediamines
An intermolecular defluorinative vicinal diamination protocol employing fluoroalkenyl iodides and sulfonamides for the efficient synthesis of a series of acyclic and cyclic fluorinated 1,2-enediamines has been developed.
Authors
- Xueying Huang (ORCID: https://orcid.org/0000-0001-8427-6394)
- Chi Zhang (ORCID: https://orcid.org/0000-0002-9018-0492)
- Xue‐Qiang Chu (ORCID: https://orcid.org/0000-0002-9173-1508)
- Zhi‐Liang Shen (ORCID: https://orcid.org/0000-0002-3365-9288)
- Danhua Ge (ORCID: https://orcid.org/0000-0002-0555-4307)
- Yulan Chen (ORCID: https://orcid.org/0000-0001-6017-8888)
- Yu Ding (ORCID: https://orcid.org/0000-0003-0546-0244)
Institutions
- Nanjing Tech University (CN)
- Xuzhou Medical College (CN)
Publication Details
- Journal
- Organic Chemistry Frontiers
- Published
- 2024-11-13
- DOI
- https://doi.org/10.1039/d4qo01913j
- Citations
- 8
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 1.66
Funders
- National Natural Science Foundation of China
- Nanjing Tech University