Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water
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-...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Article |
| Language: | en_US |
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John Wiley & Sons, Inc.
2013
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| Online Access: | http://hdl.handle.net/1721.1/82111 |
| _version_ | 1826211917015810048 |
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| author | Lou, Sha Fu, Gregory C. |
| author2 | Massachusetts Institute of Technology. Department of Chemistry |
| author_facet | Massachusetts Institute of Technology. Department of Chemistry Lou, Sha Fu, Gregory C. |
| author_sort | Lou, Sha |
| collection | MIT |
| description | 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. |
| first_indexed | 2024-09-23T15:13:09Z |
| format | Article |
| id | mit-1721.1/82111 |
| institution | Massachusetts Institute of Technology |
| language | en_US |
| last_indexed | 2024-09-23T15:13:09Z |
| publishDate | 2013 |
| publisher | John Wiley & Sons, Inc. |
| record_format | dspace |
| spelling | mit-1721.1/821112022-10-02T01:26:00Z Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water Lou, Sha Fu, Gregory C. Massachusetts Institute of Technology. Department of Chemistry Lou, Sha Fu, Gregory C. 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. National Institutes of Health (U.S.) (National Institute of General Medical Sciences, grant R01-GM62871) Merck Research Laboratories Novartis (Firm) 2013-11-15T14:17:36Z 2013-11-15T14:17:36Z 2010-07 2010-04 Article http://purl.org/eprint/type/JournalArticle 16154150 http://hdl.handle.net/1721.1/82111 Lou, Sha, and Gregory C. Fu. “Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water.” Advanced Synthesis & Catalysis 352, no. 11 12 (October 9, 2010): 2081-2084. en_US http://dx.doi.org/10.1002/adsc.201000267 Advanced Synthesis & Catalysis Creative Commons Attribution-Noncommercial-Share Alike 3.0 http://creativecommons.org/licenses/by-nc-sa/3.0/ application/pdf John Wiley & Sons, Inc. PMC |
| spellingShingle | Lou, Sha Fu, Gregory C. Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water |
| title | Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water |
| title_full | Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water |
| title_fullStr | Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water |
| title_full_unstemmed | Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water |
| title_short | Palladium/Tris(tert-butyl)phosphine-Catalyzed Suzuki Cross-Couplings in the Presence of Water |
| title_sort | palladium tris tert butyl phosphine catalyzed suzuki cross couplings in the presence of water |
| url | http://hdl.handle.net/1721.1/82111 |
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