Developing Efficient Nucleophilic Fluorination Methods and Application to Substituted Picolinate Esters-Reference-Cited by-同舟云学术

Developing Efficient Nucleophilic Fluorination Methods and Application to Substituted Picolinate Esters

Published:2014-07-16 Issue:8 Volume:18 Page:1045-1054
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Allen Laura J.¹,Lee Shin Hee¹,Cheng Yang²,Hanley Patrick S.²,Muhuhi Joseck M.²,Kane Elisabeth²,Powers Stacey L.²,Anderson John E.²,Bell Bruce M.²,Roth Gary A.²,Sanford Melanie S.¹,Bland Douglas C.²

Affiliation:

1. Department of Chemistry, University of Michigan, 930 N. University Ave, Ann Arbor, Michigan 48109, United States

2. Dow Chemical Company, 1710 Building, Midland, Michigan 48674, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op5001258

Reference26 articles.

1. The unique role of halogen substituents in the design of modern agrochemicals

2. Fluorine in medicinal chemistry

3. The Many Roles for Fluorine in Medicinal Chemistry

4. The Unique Role of Fluorine in the Design of Active Ingredients for Modern Crop Protection

5. N-Fluoro-N-alkylsulfonamides: useful reagents for the fluorination of carbanions

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