These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
165 related articles for article (PubMed ID: 17143919)
1. Biaryls made easy: PEPPSI and the Kumada-Tamao-Corriu reaction. Organ MG; Abdel-Hadi M; Avola S; Hadei N; Nasielski J; O'brien CJ; Valente C Chemistry; 2007; 13(1):150-7. PubMed ID: 17143919 [TBL] [Abstract][Full Text] [Related]
2. A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the negishi reaction: a step towards a universal cross-coupling catalyst. Organ MG; Avola S; Dubovyk I; Hadei N; Kantchev EA; O'Brien CJ; Valente C Chemistry; 2006 Jun; 12(18):4749-55. PubMed ID: 16568493 [TBL] [Abstract][Full Text] [Related]
3. Structure-activity relationship analysis of Pd-PEPPSI complexes in cross-couplings: a close inspection of the catalytic cycle and the precatalyst activation model. Nasielski J; Hadei N; Achonduh G; Kantchev EA; O'Brien CJ; Lough A; Organ MG Chemistry; 2010 Sep; 16(35):10844-53. PubMed ID: 20665575 [TBL] [Abstract][Full Text] [Related]
4. Two flavors of PEPPSI-IPr: activation and diffusion control in a single NHC-ligated Pd catalyst? Larrosa I; Somoza C; Banquy A; Goldup SM Org Lett; 2011 Jan; 13(1):146-9. PubMed ID: 21133362 [TBL] [Abstract][Full Text] [Related]
5. One-Pot Sequential Kumada-Tamao-Corriu Couplings of (Hetero)Aryl Polyhalides in the Presence of Grignard-Sensitive Functional Groups Using Pd-PEPPSI-IPent Sinha N; Champagne PA; Rodriguez MJ; Lu Y; Kopach ME; Mitchell D; Organ MG Chemistry; 2019 May; 25(26):6508-6512. PubMed ID: 30972856 [TBL] [Abstract][Full Text] [Related]
6. Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biaryls. Organ MG; Calimsiz S; Sayah M; Hoi KH; Lough AJ Angew Chem Int Ed Engl; 2009; 48(13):2383-7. PubMed ID: 19226587 [TBL] [Abstract][Full Text] [Related]
7. An efficient low-temperature Stille-Migita cross-coupling reaction for heteroaromatic compounds by Pd-PEPPSI-IPent. Dowlut M; Mallik D; Organ MG Chemistry; 2010 Apr; 16(14):4279-83. PubMed ID: 20209529 [TBL] [Abstract][Full Text] [Related]
8. Air-stable, convenient to handle Pd based PEPPSI (pyridine enhanced precatalyst preparation, stabilization and initiation) themed precatalysts of N/O-functionalized N-heterocyclic carbenes and its utility in Suzuki-Miyaura cross-coupling reaction. Ray L; Shaikh MM; Ghosh P Dalton Trans; 2007 Oct; (40):4546-55. PubMed ID: 17928912 [TBL] [Abstract][Full Text] [Related]
9. Functional group tolerant Kumada-Corriu-Tamao coupling of nonactivated alkyl halides with aryl and heteroaryl nucleophiles: catalysis by a nickel pincer complex permits the coupling of functionalized Grignard reagents. Vechorkin O; Proust V; Hu X J Am Chem Soc; 2009 Jul; 131(28):9756-66. PubMed ID: 19552426 [TBL] [Abstract][Full Text] [Related]
11. An alternative approach to PEPPSI catalysts: from palladium isonitriles to highly active unsymmetrically substituted PEPPSI catalysts. Zeiler A; Rudolph M; Rominger F; Hashmi AS Chemistry; 2015 Jul; 21(31):11065-71. PubMed ID: 26096141 [TBL] [Abstract][Full Text] [Related]
12. Pd-PEPPSI: Pd-NHC Precatalyst for Suzuki-Miyaura Cross-Coupling Reactions of Amides. Lei P; Meng G; Ling Y; An J; Szostak M J Org Chem; 2017 Jul; 82(13):6638-6646. PubMed ID: 28654258 [TBL] [Abstract][Full Text] [Related]
14. Kumada-Tamao-Corriu coupling of heteroaromatic chlorides and aryl ethers catalyzed by (IPr)Ni(allyl)Cl. Iglesias MJ; Prieto A; Nicasio MC Org Lett; 2012 Sep; 14(17):4318-21. PubMed ID: 22894704 [TBL] [Abstract][Full Text] [Related]
15. Highly active palladium catalysts supported by bulky proazaphosphatrane ligands for Stille cross-coupling: coupling of aryl and vinyl chlorides, room temperature coupling of aryl bromides, coupling of aryl triflates, and synthesis of sterically hindered biaryls. Su W; Urgaonkar S; McLaughlin PA; Verkade JG J Am Chem Soc; 2004 Dec; 126(50):16433-9. PubMed ID: 15600345 [TBL] [Abstract][Full Text] [Related]
16. Efficient synthesis of sterically crowded biaryls by palladium-phosphinous acid-catalyzed cross-coupling of aryl halides and aryl grignards. Wolf C; Xu H J Org Chem; 2008 Jan; 73(1):162-7. PubMed ID: 18052388 [TBL] [Abstract][Full Text] [Related]
17. The Kumada-Tamao-Corriu Coupling Reaction Catalyzed by Rhodium-Aluminum Bimetallic Complexes. Fujii I; Semba K; Nakao Y Org Lett; 2022 Apr; 24(16):3075-3079. PubMed ID: 35426689 [TBL] [Abstract][Full Text] [Related]
18. High efficiency of cavity-based triaryl-phosphines in nickel-catalysed Kumada-Tamao-Corriu cross-coupling. Monnereau L; Sémeril D; Matt D Chem Commun (Camb); 2011 Jun; 47(23):6626-8. PubMed ID: 21544285 [TBL] [Abstract][Full Text] [Related]
19. Pd-PEPPSI-IPent: low-temperature negishi cross-coupling for the preparation of highly functionalized, tetra-ortho-substituted biaryls. Calimsiz S; Sayah M; Mallik D; Organ MG Angew Chem Int Ed Engl; 2010 Mar; 49(11):2014-7. PubMed ID: 20162639 [No Abstract] [Full Text] [Related]
20. Synthesis of tetra-ortho-substituted, phosphorus-containing and carbonyl-containing biaryls utilizing a Diels-Alder approach. Ashburn BO; Carter RG; Zakharov LN J Am Chem Soc; 2007 Jul; 129(29):9109-16. PubMed ID: 17602479 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]