111 related articles for article (PubMed ID: 20481437)
1. i-PrI acceleration of Negishi cross-coupling reactions.
Kienle M; Knochel P
Org Lett; 2010 Jun; 12(12):2702-5. PubMed ID: 20481437
[TBL] [Abstract][Full Text] [Related]
2. Structure-reactivity relationships in negishi cross-coupling reactions.
Dong ZB; Manolikakes G; Shi L; Knochel P; Mayr H
Chemistry; 2010 Jan; 16(1):248-53. PubMed ID: 19904779
[TBL] [Abstract][Full Text] [Related]
3. Negishi cross-coupling reactions catalyzed by an aminophosphine-based nickel system: a reliable and general applicable reaction protocol for the high-yielding synthesis of biaryls.
Gerber R; Frech CM
Chemistry; 2011 Oct; 17(42):11893-904. PubMed ID: 21887715
[TBL] [Abstract][Full Text] [Related]
4. One-pot Negishi cross-coupling reactions of in situ generated zinc reagents with aryl chlorides, bromides, and triflates.
Sase S; Jaric M; Metzger A; Malakhov V; Knochel P
J Org Chem; 2008 Sep; 73(18):7380-2. PubMed ID: 18693766
[TBL] [Abstract][Full Text] [Related]
5. Palladium-phosphinous acid-catalyzed cross-coupling of aryl and acyl halides with aryl-, alkyl-, and vinylzinc reagents.
Xu H; Ekoue-Kovi K; Wolf C
J Org Chem; 2008 Oct; 73(19):7638-50. PubMed ID: 18767805
[TBL] [Abstract][Full Text] [Related]
6. Mild Cobalt-Catalyzed Negishi Cross-Couplings of (Hetero)arylzinc Reagents with (Hetero)aryl Halides.
Haas D; Hammann JM; Lutter FH; Knochel P
Angew Chem Int Ed Engl; 2016 Mar; 55(11):3809-12. PubMed ID: 26879151
[TBL] [Abstract][Full Text] [Related]
7. Single-electron-transfer-induced coupling of arylzinc reagents with aryl and alkenyl halides.
Shirakawa E; Tamakuni F; Kusano E; Uchiyama N; Konagaya W; Watabe R; Hayashi T
Angew Chem Int Ed Engl; 2014 Jan; 53(2):521-5. PubMed ID: 24282160
[TBL] [Abstract][Full Text] [Related]
8. Efficient Negishi coupling reactions of aryl chlorides catalyzed by binuclear and mononuclear nickel-N-heterocyclic carbene complexes.
Xi Z; Zhou Y; Chen W
J Org Chem; 2008 Nov; 73(21):8497-501. PubMed ID: 18841915
[TBL] [Abstract][Full Text] [Related]
9. Negishi cross-couplings of unsaturated halides bearing relatively acidic hydrogen atoms with organozinc reagents.
Manolikakes G; Schade MA; Hernandez CM; Mayr H; Knochel P
Org Lett; 2008 Jul; 10(13):2765-8. PubMed ID: 18529011
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Pd(PPh3)4-PEG 400 catalyzed protocol for the atom-efficient Stille cross-coupling reaction of organotin with aryl bromides.
Zhou WJ; Wang KH; Wang JX
J Org Chem; 2009 Aug; 74(15):5599-602. PubMed ID: 19552378
[TBL] [Abstract][Full Text] [Related]
12. Effective Pd-nanoparticle (PdNP)-catalyzed Negishi coupling involving alkylzinc reagents at room temperature.
Liu J; Deng Y; Wang H; Zhang H; Yu G; Wu B; Zhang H; Li Q; Marder TB; Yang Z; Lei A
Org Lett; 2008 Jul; 10(13):2661-4. PubMed ID: 18507385
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of aryl- and heteroaryl-substituted 3-benzyloxyisothiazoles via Suzuki and Negishi cross-coupling reactions.
Kaae BH; Krogsgaard-Larsen P; Johansen TN
J Org Chem; 2004 Feb; 69(4):1401-4. PubMed ID: 14961704
[TBL] [Abstract][Full Text] [Related]
14. Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates.
Zhou J; Fu GC
J Am Chem Soc; 2003 Oct; 125(41):12527-30. PubMed ID: 14531697
[TBL] [Abstract][Full Text] [Related]
15. Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalyst.
Hadei N; Kantchev EA; O'Brien CJ; Organ MG
J Org Chem; 2005 Oct; 70(21):8503-7. PubMed ID: 16209599
[TBL] [Abstract][Full Text] [Related]
16. Identification of a highly efficient alkylated pincer thioimido-palladium(II) complex as the active catalyst in Negishi coupling.
Liu J; Wang H; Zhang H; Wu X; Zhang H; Deng Y; Yang Z; Lei A
Chemistry; 2009; 15(17):4437-45. PubMed ID: 19288479
[TBL] [Abstract][Full Text] [Related]
17. Cobalt-catalyzed negishi cross-coupling reactions of (hetero)arylzinc reagents with primary and secondary alkyl bromides and iodides.
Hammann JM; Haas D; Knochel P
Angew Chem Int Ed Engl; 2015 Apr; 54(15):4478-81. PubMed ID: 25694155
[TBL] [Abstract][Full Text] [Related]
18. Efficient cross-coupling of aryl chlorides with arylzinc reagents catalyzed by amido pincer complexes of nickel.
Wang L; Wang ZX
Org Lett; 2007 Oct; 9(21):4335-8. PubMed ID: 17887695
[TBL] [Abstract][Full Text] [Related]
19. Nickel 0-catalyzed cross-coupling of alkyl arenesulfonates with aryl Grignard reagents.
Cho CH; Yun HS; Park K
J Org Chem; 2003 Apr; 68(8):3017-25. PubMed ID: 12688768
[TBL] [Abstract][Full Text] [Related]
20. Cobalt-Xantphos-catalyzed, LiCl-mediated preparation of arylzinc reagents from aryl iodides, bromides, and chlorides.
Jin MY; Yoshikai N
J Org Chem; 2011 Apr; 76(7):1972-8. PubMed ID: 21384804
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
