Exploiting a “Beast” in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy-Reference-Cited by-同舟云学术

Exploiting a “Beast” in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy

Published:2017-09-15 Issue:39 Volume:139 Page:13648-13651
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Parisi Giovanna¹²,Colella Marco¹,Monticelli Serena²,Romanazzi Giuseppe³^ORCID,Holzer Wolfgang²,Langer Thierry²,Degennaro Leonardo¹^ORCID,Pace Vittorio²,Luisi Renzo¹^ORCID

Affiliation:

1. Department of Pharmacy − Drug Sciences, University of Bari “A. Moro”, Via E. Orabona 4, 70125 Bari, Italy

2. Department of Pharmaceutical Chemistry, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria

3. DICATECh, Politecnico di Bari, Via E. Orabona 4, 70125 Bari, Italy

Funder

Universita degli Studi di Bari Aldo Moro

Universit?t Wien

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.7b07891

Reference54 articles.

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2. Fluorine in Pharmaceutical Industry: Fluorine-Containing Drugs Introduced to the Market in the Last Decade (2001–2011)

3. Applications of Fluorine in Medicinal Chemistry

4. Transition metal catalysis and nucleophilic fluorination

5. Late-stage [18F]fluorination: new solutions to old problems

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