Metal-Free and User-Friendly Regioselective Hydroxyfluorination of Olefins-Reference-Cited by-同舟云学术

Metal-Free and User-Friendly Regioselective Hydroxyfluorination of Olefins

Published:2018-04-06 Issue:8 Volume:20 Page:2338-2341
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Sedgwick Daniel M.¹²,López Inés¹,Román Raquel²,Kobayashi Nanako³,Okoromoba Otome E.⁴,Xu Bo⁵^ORCID,Hammond Gerald B.⁴^ORCID,Barrio Pablo¹,Fustero Santos¹²^ORCID

Affiliation:

1. Departamento de Química Orgánica, Universidad de Valencia, E-46100 Burjassot, Spain

2. Laboratorio de Moléculas Orgánicas, Centro de Investigación Príncipe Felipe, E-46012 Valencia, Spain

3. Department of Chemistry, Faculty of Science, Gakushuin University, 1-5-1 Mejiro, Toshima-ku, Tokyo 171-8588, Japan

4. Department of Chemistry, University of Louisville, Louisville, Kentucky 40292, United States

5. College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, China

Funder

Generalitat Valenciana

Ministerio de Econom?a y Competitividad

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b00681

Reference53 articles.

1. Pd-Catalyzed Regioselective 1,2-Difunctionalization of Vinylarenes with Alkenyl Triflates and Aryl Boronic Acids at Ambient Temperature

2. Pd-Catalyzed Regioselective 1,2-Dicarbofunctionalization of Unactivated Olefins by a Heck Reaction/Enolate Cyclization Cascade

3. Iron-Catalyzed Intermolecular 1,2-Difunctionalization of Styrenes and Conjugated Alkenes with Silanes and Nucleophiles

4. Searching for New Reactivity (Nobel Lecture) Copyright© The Nobel Foundation 2002. We thank the Nobel Foundation, Stockholm, for permission to print this lecture. Adapted with the permission of the editors from “Coelacanths and Catalysis”: K. B. Sharpless, Tetrahedron 1994, 50, 4235.

5. Organofluorine Compounds

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