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Decarboxylative Fluorination Strategies for Accessing Medicinally-relevant Products
Qiao, Yupu Zhu, Lingui Ambler, Brett R. Altman, Ryan A.
Qiao, Yupu
Zhu, Lingui
Ambler, Brett R.
Altman, Ryan A.
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Abstract
Fluorinated organic compounds have a long history in medicinal chemistry, and synthetic methods to access target fluorinated compounds are undergoing a revolution. One powerful strategy for the installation of fluorine-containing functional groups includes decarboxylative reactions. Benefits of decarboxylative approaches potentially include: 1) readily available substrates or reagents 2) mild reaction conditions; 3) simplified purification. This focus review highlights the applications of decarboxylation strategies for fluorination reactions to access compounds with biomedical potential. The manuscript highlights on two general strategies, fluorination by decarboxylative reagents and by decarboxylation of substrates. Where relevant, examples of medicinally useful compounds that can be accessed using these strategies are highlighted.
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Date
2015-01-01
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Bentham Science Publishers
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Keywords
Decarboxylation, Fluorination, Difluoromethylation, Trifluoromethylation, Copper
Citation
Qiao, Yupu, Lingui Zhu, Brett Ambler, and Ryan Altman. "Decarboxylative Fluorination Strategies for Accessing Medicinally- Relevant Products." Current Topics in Medicinal Chemistry 14.7 (2014): 966-78.