204 related articles for article (PubMed ID: 21553878)
1. Nickel-catalyzed Kumada cross-coupling reactions of tertiary alkylmagnesium halides and aryl bromides/triflates.
Joshi-Pangu A; Wang CY; Biscoe MR
J Am Chem Soc; 2011 Jun; 133(22):8478-81. PubMed ID: 21553878
[TBL] [Abstract][Full Text] [Related]
2. Stereoretentive Pd-catalysed Stille cross-coupling reactions of secondary alkyl azastannatranes and aryl halides.
Li L; Wang CY; Huang R; Biscoe MR
Nat Chem; 2013 Jul; 5(7):607-12. PubMed ID: 23787752
[TBL] [Abstract][Full Text] [Related]
3. Visible-Light-Promoted Nickel- and Organic-Dye-Cocatalyzed Formylation Reaction of Aryl Halides and Triflates and Vinyl Bromides with Diethoxyacetic Acid as a Formyl Equivalent.
Huang H; Li X; Yu C; Zhang Y; Mariano PS; Wang W
Angew Chem Int Ed Engl; 2017 Feb; 56(6):1500-1505. PubMed ID: 28066982
[TBL] [Abstract][Full Text] [Related]
4. Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chlorides.
Everson DA; Jones BA; Weix DJ
J Am Chem Soc; 2012 Apr; 134(14):6146-59. PubMed ID: 22463689
[TBL] [Abstract][Full Text] [Related]
5. The Use of Tertiary Alkylmagnesium Nucleophiles in Ni-Catalyzed Cross-Coupling Reactions.
Joshi-Pangu A; Biscoe MR
Synlett; 2012 May; 23(8):1103-1107. PubMed ID: 23641126
[TBL] [Abstract][Full Text] [Related]
6. Controlling Ni redox states by dynamic ligand exchange for electroreductive Csp3-Csp2 coupling.
Hamby TB; LaLama MJ; Sevov CS
Science; 2022 Apr; 376(6591):410-416. PubMed ID: 35446658
[TBL] [Abstract][Full Text] [Related]
7. Magnesiation of electron-rich aryl bromides and their use in nickel-catalyzed cross-coupling reactions.
Lau SY; Hughes G; O'Shea PD; Davies IW
Org Lett; 2007 May; 9(11):2239-42. PubMed ID: 17480092
[TBL] [Abstract][Full Text] [Related]
8. Unsymmetrical diaryl sulfones and aryl vinyl sulfones through palladium-catalyzed coupling of aryl and vinyl halides or triflates with sulfinic acid salts.
Cacchi S; Fabrizi G; Goggiamani A; Parisi LM; Bernini R
J Org Chem; 2004 Aug; 69(17):5608-14. PubMed ID: 15307729
[TBL] [Abstract][Full Text] [Related]
9. Methods and Mechanisms for Cross-Electrophile Coupling of Csp(2) Halides with Alkyl Electrophiles.
Weix DJ
Acc Chem Res; 2015 Jun; 48(6):1767-75. PubMed ID: 26011466
[TBL] [Abstract][Full Text] [Related]
10. Atom-efficient metal-catalyzed cross-coupling reaction of indium organometallics with organic electrophiles.
Pérez I; Sestelo JP; Sarandeses LA
J Am Chem Soc; 2001 May; 123(18):4155-60. PubMed ID: 11457178
[TBL] [Abstract][Full Text] [Related]
11. Nickel-Catalyzed Reductive Coupling of Aryl Bromides with Tertiary Alkyl Halides.
Wang X; Wang S; Xue W; Gong H
J Am Chem Soc; 2015 Sep; 137(36):11562-5. PubMed ID: 26325479
[TBL] [Abstract][Full Text] [Related]
12. Nickel-catalyzed biaryl coupling of heteroarenes and aryl halides/triflates.
Canivet J; Yamaguchi J; Ban I; Itami K
Org Lett; 2009 Apr; 11(8):1733-6. PubMed ID: 19296639
[TBL] [Abstract][Full Text] [Related]
13. Nickel-catalyzed vinylation of aryl chlorides and bromides with vinyl ZnBr.MgBrCl.
Yamamoto T; Yamakawa T
J Org Chem; 2009 May; 74(9):3603-5. PubMed ID: 19354270
[TBL] [Abstract][Full Text] [Related]
14. Nickel-catalyzed decarboxylative cross-coupling of perfluorobenzoates with aryl halides and sulfonates.
Sardzinski LW; Wertjes WC; Schnaith AM; Kalyani D
Org Lett; 2015 Mar; 17(5):1256-9. PubMed ID: 25700128
[TBL] [Abstract][Full Text] [Related]
15. Dual nickel- and photoredox-catalyzed reductive cross-coupling of aryl vinyl halides and unactivated tertiary alkyl bromides.
Yu W; Chen L; Tao J; Wang T; Fu J
Chem Commun (Camb); 2019 May; 55(42):5918-5921. PubMed ID: 31045192
[TBL] [Abstract][Full Text] [Related]
16. Cross-Couplings Using Aryl Ethers via C-O Bond Activation Enabled by Nickel Catalysts.
Tobisu M; Chatani N
Acc Chem Res; 2015 Jun; 48(6):1717-26. PubMed ID: 26036674
[TBL] [Abstract][Full Text] [Related]
17. Ni/Photoredox-Catalyzed C(sp
Cauley AN; Ramirez A; Barhate CL; Donnell AF; Khandelwal P; Sezen-Edmonds M; Sherwood TC; Sloane JL; Cavallaro CL; Simmons EM
Org Lett; 2022 Aug; 24(31):5663-5668. PubMed ID: 35920644
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Multimetallic catalysed cross-coupling of aryl bromides with aryl triflates.
Ackerman LK; Lovell MM; Weix DJ
Nature; 2015 Aug; 524(7566):454-7. PubMed ID: 26280337
[TBL] [Abstract][Full Text] [Related]
20. Preparation of Vinyl Arenes by Nickel-Catalyzed Reductive Coupling of Aryl Halides with Vinyl Bromides.
Liu J; Ren Q; Zhang X; Gong H
Angew Chem Int Ed Engl; 2016 Dec; 55(50):15544-15548. PubMed ID: 27862759
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
