Published October 9, 2010
| Accepted Version + Supplemental Material
Journal Article
Open
Palladium/Tris(tert-butyl)phosphine‐Catalyzed Suzuki Cross‐ Couplings in the Presence of Water
- Creators
- Lou, Sha
-
Fu, Gregory C.
Abstract
Dipalladiumtris(dibenzylideneacetone)/tris(tert‐butyl)phosphonium tetrafluoroborate/potassium fluoride dihydrate [Pd₂(dba)₃/[HP(t‐Bu)₃]BF₄/KF⋅2 H₂O] serves as a mild, robust, and user‐friendly method for the efficient Suzuki cross‐coupling of a diverse array of aryl and heteroaryl halides with aryl‐ and heteroarylboronic acids.
Additional Information
© 2010 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. Received: April 5, 2010; Published online: July 21, 2010. Support has been provided by the National Institutes of Health (National Institute of General Medical Sciences, grant R01‐GM62871), Merck Research Laboratories, and Novartis. We thank Dr. Xing Dai for a preliminary study.Attached Files
Accepted Version - nihms257833.pdf
Supplemental Material - adsc_201000267_sm_miscellaneous_information.pdf
Files
nihms257833.pdf
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Additional details
- Alternative title
- Pd/P(t-Bu)(3)-Catalyzed Suzuki Cross-Couplings in the Presence of Water
- PMCID
- PMC3011868
- Eprint ID
- 103170
- DOI
- 10.1002/adsc.201000267
- Resolver ID
- CaltechAUTHORS:20200513-095516372
- R01‐GM62871
- NIH
- Merck Research Laboratories
- Novartis
- Created
-
2020-05-13Created from EPrint's datestamp field
- Updated
-
2021-11-16Created from EPrint's last_modified field