Deoxytrifluoromethylation/aromatization of cyclohexan(en)ones to access highly substituted trifluoromethyl arenes-Reference-Cited by-同舟云学术

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Deoxytrifluoromethylation/aromatization of cyclohexan(en)ones to access highly substituted trifluoromethyl arenes

Published:2024-09-09 Issue:1 Volume:15 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Bhattarai Pankaj^ORCID,Abd El-Gaber Mohammed K.^ORCID,Koley Suvajit,Altman Ryan A.^ORCID

Funder

U.S. Department of Health & Human Services | NIH | National Cancer Institute

National Science Foundation

U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences

Steve and Lee Ann Taglienti Endowment

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s41467-024-52035-9.pdf

Reference47 articles.

1. Dolbier, W. R. Fluorine chemistry at the millennium. J. Fluor. Chem. 126, 157–163 (2005).

2. Maienfisch, P. & Hall, R. G. The Importance of Fluorine in the Life Science Industry. Chimia 58, 93 (2004).

3. Richardson, P. Fluorination methods for drug discovery and development. Expert Opin. Drug Discov. 11, 983–999 (2016).

4. Shah, P. & Westwell, A. D. The role of fluorine in medicinal chemistry. J. Enzym. Inhibition Medicinal Chem. 22, 527–540 (2007).

5. Jeschke, P. The Unique Role of Fluorine in the Design of Active Ingredients for Modern Crop Protection. ChemBioChem 5, 570–589 (2004).

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