Substituent Effects on Aryltrifluoroborate Solvolysis in Water: Implications for Suzuki−Miyaura Coupling and the Design of Stable 18F-Labeled Aryltrifluoroborates for Use in PET Imaging-Reference-Cited by-同舟云学术

Substituent Effects on Aryltrifluoroborate Solvolysis in Water: Implications for Suzuki−Miyaura Coupling and the Design of Stable 18F-Labeled Aryltrifluoroborates for Use in PET Imaging

Published:2008-05-20 Issue:12 Volume:73 Page:4662-4670
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ting Richard¹,Harwig Curtis W.¹,Lo Justin¹,Li Ying¹,Adam Michael J.¹,Ruth Thomas J.¹,Perrin David M.¹

Affiliation:

1. Chemistry Department, University of British Columbia, 2036 Main Mall, and TRIUMF Vancouver, B.C. V6T-1Z1, Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800681d

Reference60 articles.

1. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Potassium Aryl- and Heteroaryltrifluoroborates

2. Fluoride-Mediated Boronic Acid Coupling Reactions

3. Conversion of Arylboronic Acids into Potassium Aryltrifluoroborates: Convenient Precursors of Arylboron Difluoride Lewis Acids

4. Suzuki−Miyaura Cross-Coupling Reactions of Potassium Alkenyltrifluoroborates

5. Synthesis and cross-coupling reactions of tetraalkylammonium organotrifluoroborate salts

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