284 related articles for article (PubMed ID: 12583734)
1. Highly efficient, general procedure for the preparation of alkylzinc reagents from unactivated alkyl bromides and chlorides.
Huo S
Org Lett; 2003 Feb; 5(4):423-5. PubMed ID: 12583734
[TBL] [Abstract][Full Text] [Related]
2. Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).
Terao J; Kambe N
Acc Chem Res; 2008 Nov; 41(11):1545-54. PubMed ID: 18973349
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Efficient Stille cross-coupling reaction catalyzed by the Pd(OAc)2/Dabco catalytic system.
Li JH; Liang Y; Wang DP; Liu WJ; Xie YX; Yin DL
J Org Chem; 2005 Apr; 70(7):2832-4. PubMed ID: 15787581
[TBL] [Abstract][Full Text] [Related]
6. Cobalt-catalyzed reductive coupling of saturated alkyl halides with activated alkenes.
Shukla P; Hsu YC; Cheng CH
J Org Chem; 2006 Jan; 71(2):655-8. PubMed ID: 16408976
[TBL] [Abstract][Full Text] [Related]
7. Palladium-catalyzed cross-coupling reactions between dihydropyranylindium reagents and aryl halides. synthesis of C-aryl glycals.
Lehmann U; Awasthi S; Minehan T
Org Lett; 2003 Jul; 5(14):2405-8. PubMed ID: 12841741
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A general preparation of polyfunctional benzylic zinc organometallic compounds.
Metzger A; Schade MA; Manolikakes G; Knochel P
Chem Asian J; 2008 Sep; 3(8-9):1678-91. PubMed ID: 18604829
[TBL] [Abstract][Full Text] [Related]
10. Preparation of functionalized organoindium reagents by means of magnesium insertion into organic halides in the presence of InCl3 at room temperature.
Bernhardt S; Shen ZL; Knochel P
Chemistry; 2013 Jan; 19(3):828-33. PubMed ID: 23255158
[TBL] [Abstract][Full Text] [Related]
11. Preparation of highly functionalized alkylzinc halides from alkyl bromides using Mg, ZnCl2 and LiCl.
Blümke TD; Piller FM; Knochel P
Chem Commun (Camb); 2010 Jun; 46(23):4082-4. PubMed ID: 20379592
[TBL] [Abstract][Full Text] [Related]
12. (t-Bu)2PN=P(i-BuNCH2CH2)3N: new efficient ligand for palladium-catalyzed C-N couplings of aryl and heteroaryl bromides and chlorides and for vinyl bromides at room temperature.
Reddy ChV; Kingston JV; Verkade JG
J Org Chem; 2008 Apr; 73(8):3047-62. PubMed ID: 18370424
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Nickel-catalyzed cross-coupling reactions of benzylic zinc reagents with aromatic bromides, chlorides and tosylates.
Schade MA; Metzger A; Hug S; Knochel P
Chem Commun (Camb); 2008 Jul; (26):3046-8. PubMed ID: 18688343
[TBL] [Abstract][Full Text] [Related]
15. Efficient cross-coupling of functionalized arylzinc halides catalyzed by a nickel chloride-diethyl phosphite system.
Gavryushin A; Kofink C; Manolikakes G; Knochel P
Org Lett; 2005 Oct; 7(22):4871-4. PubMed ID: 16235910
[TBL] [Abstract][Full Text] [Related]
16. Functionalized arylzinc compounds in ethereal solvent: direct synthesis from aryl iodides and zinc powder and application to Pd-catalyzed reaction with allylic halides.
Ikegami R; Koresawa A; Shibata T; Takagi K
J Org Chem; 2003 Mar; 68(6):2195-9. PubMed ID: 12636380
[TBL] [Abstract][Full Text] [Related]
17. Catalytic asymmetric addition of alkylzinc and functionalized alkylzinc reagents to ketones.
Jeon SJ; Li H; García C; LaRochelle LK; Walsh PJ
J Org Chem; 2005 Jan; 70(2):448-55. PubMed ID: 15651785
[TBL] [Abstract][Full Text] [Related]
18. 9-fluorenylphosphines for the Pd-catalyzed sonogashira, suzuki, and Buchwald-Hartwig coupling reactions in organic solvents and water.
Fleckenstein CA; Plenio H
Chemistry; 2007; 13(9):2701-16. PubMed ID: 17200923
[TBL] [Abstract][Full Text] [Related]
19. Guanidine/Pd(OAc)2-catalyzed room temperature Suzuki cross-coupling reaction in aqueous media under aerobic conditions.
Li S; Lin Y; Cao J; Zhang S
J Org Chem; 2007 May; 72(11):4067-72. PubMed ID: 17465565
[TBL] [Abstract][Full Text] [Related]
20. Cross-coupling and dehalogenation reactions catalyzed by (N-heterocyclic carbene)Pd(allyl)Cl complexes.
Navarro O; Kaur H; Mahjoor P; Nolan SP
J Org Chem; 2004 Apr; 69(9):3173-80. PubMed ID: 15104459
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
