Talk:Dialkylbiaryl phosphine ligands

Trim the primary refs, or most of them
The topic has been reviewed in 2007, so references discussed in the review are not needed for this overview. See WP:SECONDARY.

1.	 Kaye, Steven; Fox, Joseph M.; Hicks, Frederick A.; Buchwald, Stephen L. (31 December 2001). "The Use of Catalytic Amounts of CuCl and Other Improvements in the Benzyne Route to Biphenyl-Based Phosphine Ligands". Advanced Synthesis & Catalysis. 343(8): 789–794. doi:10.1002/1615-4169(20011231)343:8<789::AID-ADSC789>3.0.CO;2-A. ISSN 1615-4169.

2.	^ Martin, Ruben; Buchwald, Stephen L. (18 November 2008). "Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands". Accounts of Chemical Research. 41 (11): 1461–1473. doi:10.1021/ar800036s. ISSN 0001-4842. PMC 2645945. PMID 18620434.

3.	^ Biscoe, Mark R.; Fors, Brett P.; Buchwald, Stephen L. (2008-05-01). "A New Class of Easily Activated Palladium Precatalysts for Facile C−N Cross-Coupling Reactions and the Low Temperature Oxidative Addition of Aryl Chlorides". Journal of the American Chemical Society. 130 (21): 6686–6687. doi:10.1021/ja801137k. PMC 2587037. PMID 18447360.

4.	^ Bruno, N. C.; Buchwald, S. L. (2014). Palladium Precatalysts for Cross-Coupling Reactions (PDF). The Strem Chemiker.

5.	 Old, David W.; Wolfe, John P.; Buchwald, Stephen L. (September 1998). "A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides". Journal of the American Chemical Society. 120 (37): 9722–9723. doi:10.1021/ja982250+.

6.	Fox, Joseph M.; Huang, Xiaohua; Chieffi, André; Buchwald, Stephen L. (1 February 2000). "Highly Active and Selective Catalysts for the Formation of α-Aryl Ketones". Journal of the American Chemical Society. 122 (7): 1360–1370. doi:10.1021/ja993912d. ISSN 0002-7863.

7.	^ Moradi, Wahed A.; Buchwald, Stephen L. (2001). "Palladium-Catalyzedα-Arylation of Esters". Journal of the American Chemical Society. 123 (33): 7996–8002. doi:10.1021/ja010797+. ISSN 0002-7863. PMID 11506555. 8.	^ Billingsley, Kelvin L.; Barder, Timothy E.; Buchwald, Stephen L. (9 July 2007). "Palladium-Catalyzed Borylation of Aryl Chlorides: Scope, Applications, and Computational Studies". Angewandte Chemie International Edition. 46 (28): 5359–5363. doi:10.1002/anie.200701551. ISSN 1521-3773. PMID 17562550.

9.	^ Old, David W.; Harris, Michele C.; Buchwald, Stephen L. (1 May 2000). "Efficient Palladium-Catalyzed N-Arylation of Indoles". Organic Letters. 2 (10): 1403–1406. doi:10.1021/ol005728z. ISSN 1523-7060. PMID 10814458.

10.	^ Wolfe, John P.; Singer, Robert A.; Yang, Bryant H.; Buchwald, Stephen L. (1 October 1999). "Highly Active Palladium Catalysts for Suzuki Coupling Reactions". Journal of the American Chemical Society. 121 (41): 9550–9561. doi:10.1021/ja992130h. ISSN 0002-7863.

11.	^ Wolfe, John P.; Singer, Robert A.; Yang, Bryant H.; Buchwald, Stephen L. (1 October 1999). "Highly Active Palladium Catalysts for Suzuki Coupling Reactions". Journal of the American Chemical Society. 121 (41): 9550–9561. doi:10.1021/ja992130h. ISSN 0002-7863.

12.	^ Wolfe, John P.; Tomori, Hiroshi; Sadighi, Joseph P.; Yin, Jingjun; Buchwald, Stephen L. (1 February 2000). "Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates" (PDF). The Journal of Organic Chemistry. 65 (4): 1158–1174. doi:10.1021/jo991699y. ISSN 0022-3263. PMID 10814067.

13.	^ Surry, David S.; Buchwald, Stephen L. (11 August 2008). "Biaryl Phosphane Ligands in Palladium-Catalyzed Amination". Angewandte Chemie International Edition. 47 (34): 6338–6361. doi:10.1002/anie.200800497. ISSN 1521-3773. PMC 3517088. PMID 18663711.

14.	 Okazawa, Toru; Satoh, Tetsuya; Miura, Masahiro; Nomura, Masakatsu (1 May 2002). "Palladium-Catalyzed Multiple Arylation of Thiophenes". Journal of the American Chemical Society. 124(19): 5286–5287. doi:10.1021/ja0259279. ISSN 0002-7863. PMID 11996567.

15.	^ Wolfe, John P.; Singer, Robert A.; Yang, Bryant H.; Buchwald, Stephen L. (1 October 1999). "Highly Active Palladium Catalysts for Suzuki Coupling Reactions". Journal of the American Chemical Society. 121 (41): 9550–9561. doi:10.1021/ja992130h. ISSN 0002-7863.

16.	^ Fox, Joseph M.; Huang, Xiaohua; Chieffi, André; Buchwald, Stephen L. (1 February 2000). "Highly Active and Selective Catalysts for the Formation of α-Aryl Ketones". Journal of the American Chemical Society. 122 (7): 1360–1370. doi:10.1021/ja993912d. ISSN 0002-7863.

17.	^ Thiel, Oliver; Achmatowicz, Michal; Milburn, Robert (11 June 2012). "Process Research and Development for Heterocyclic p38 MAP Kinase Inhibitors". Synlett. 23 (11): 1564–1574. doi:10.1055/s-0031-1290425.

18.	 Huang, Xiaohua; Anderson, Kevin W.; Zim, Danilo; Jiang, Lei; Klapars, Artis; Buchwald, Stephen L. (1 June 2003). "Expanding Pd-Catalyzed C−N Bond-Forming Processes: The First Amidation of Aryl Sulfonates, Aqueous Amination, and Complementarity with Cu-Catalyzed Reactions". Journal of the American Chemical Society. 125 (22): 6653–6655. doi:10.1021/ja035483w. ISSN 0002-7863. PMID 12769573.

19.	^ Billingsley, Kelvin L.; Barder, Timothy E.; Buchwald, Stephen L. (9 July 2007). "Palladium-Catalyzed Borylation of Aryl Chlorides: Scope, Applications, and Computational Studies". Angewandte Chemie International Edition. 46 (28): 5359–5363. doi:10.1002/anie.200701551. ISSN 1521-3773. PMID 17562550.

20.	 ^ Burgos, Carlos H.; Barder, Timothy E.; Huang, Xiaohua; Buchwald, Stephen L. (26 June 2006). "Significantly Improved Method for the Pd-Catalyzed Coupling of Phenols with Aryl Halides: Understanding Ligand Effects". Angewandte Chemie International Edition. 45 (26): 4321–4326. doi:10.1002/anie.200601253. ISSN 1521-3773. PMID 16733839.

21.	^ Anderson, Kevin W.; Buchwald, Stephen L. (26 September 2005). "General Catalysts for the Suzuki–Miyaura and Sonogashira Coupling Reactions of Aryl Chlorides and for the Coupling of Challenging Substrate Combinations in Water". Angewandte Chemie International Edition. 44 (38): 6173–6177. doi:10.1002/anie.200502017. ISSN 1521-3773. PMID 16097019.

22.	^ Walker, Shawn D.; Barder, Timothy E.; Martinelli, Joseph R.; Buchwald, Stephen L. (26 March 2004). "A Rationally Designed Universal Catalyst for Suzuki–Miyaura Coupling Processes". Angewandte Chemie International Edition. 43 (14): 1871–1876. doi:10.1002/anie.200353615. ISSN 1521-3773. PMID 15054800.

23.	^ Billingsley, Kelvin L.; Barder, Timothy E.; Buchwald, Stephen L. (9 July 2007). "Palladium-Catalyzed Borylation of Aryl Chlorides: Scope, Applications, and Computational Studies". Angewandte Chemie International Edition. 46 (28): 5359–5363. doi:10.1002/anie.200701551. ISSN 1521-3773. PMID 17562550.

24.	 ^ Anderson, Kevin W.; Buchwald, Stephen L. (26 September 2005). "General Catalysts for the Suzuki–Miyaura and Sonogashira Coupling Reactions of Aryl Chlorides and for the Coupling of Challenging Substrate Combinations in Water". Angewandte Chemie International Edition. 44 (38): 6173–6177. doi:10.1002/anie.200502017. ISSN 1521-3773. PMID 16097019.

25.	^ Carret, Sébastien; Deprés, Jean-Pierre (10 September 2007). "Access to Guaianolides: Highly Efficient Stereocontrolled Total Synthesis of (±)-Geigerin". Angewandte Chemie International Edition. 46 (36): 6870–6873. doi:10.1002/anie.200702031. ISSN 1521-3773. PMID 17676568.

26.	^ Milne, Jacqueline E.; Buchwald, Stephen L. (1 October 2004). "An Extremely Active Catalyst for the Negishi Cross-Coupling Reaction". Journal of the American Chemical Society. 126 (40): 13028–13032. doi:10.1021/ja0474493. ISSN 0002-7863. PMID 15469301.

27.	^ Cho, Eun Jin; Senecal, Todd D.; Kinzel, Tom; Zhang, Yong; Watson, Donald A.; Buchwald, Stephen L. (25 June 2010). "The Palladium-Catalyzed Trifluoromethylation of Aryl Chlorides". Science. 328 (5986): 1679–1681. Bibcode:2010Sci...328.1679C. doi:10.1126/science.1190524. ISSN 0036-8075. PMC 3005208. PMID 20576888.

28.	 Charles, Mark D.; Schultz, Phillip; Buchwald, Stephen L. (1 September 2005). "Efficient Pd-Catalyzed Amination of Heteroaryl Halides". Organic Letters. 7 (18): 3965–3968. doi:10.1021/ol0514754. ISSN 1523-7060. PMID 16119943. --Smokefoot (talk) 22:36, 3 December 2022 (UTC)