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Journal Abstract Search

1386 related items for PubMed ID: 18370424

  • 1. (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 18; 73(8):3047-62. PubMed ID: 18370424
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  • 2. Application of a new bicyclic triaminophosphine ligand in Pd-catalyzed Buchwald-Hartwig amination reactions of aryl chlorides, bromides, and iodides.
    Urgaonkar S, Xu JH, Verkade JG.
    J Org Chem; 2003 Oct 31; 68(22):8416-23. PubMed ID: 14575466
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  • 3. Palladium-catalyzed cross-coupling reactions of amines with alkenyl bromides: a new method for the synthesis of enamines and imines.
    Barluenga J, Fernández MA, Aznar F, Valdés C.
    Chemistry; 2004 Jan 23; 10(2):494-507. PubMed ID: 14735518
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  • 4. Scope and limitations of Pd2(dba)3/P(i-BuNCH2CH2)3N-catalyzed Buchwald-Hartwig amination reactions of aryl chlorides.
    Urgaonkar S, Verkade JG.
    J Org Chem; 2004 Dec 24; 69(26):9135-42. PubMed ID: 15609947
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  • 5. 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 22; 126(50):16433-9. PubMed ID: 15600345
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  • 6. Simple amine/Pd(OAc)(2)-catalyzed suzuki coupling reactions of aryl bromides under mild aerobic conditions.
    Tao B, Boykin DW.
    J Org Chem; 2004 Jun 25; 69(13):4330-5. PubMed ID: 15202886
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  • 9. 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 14; 70(21):8503-7. PubMed ID: 16209599
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  • 11. Aqueous-phase, palladium-catalyzed cross-coupling of aryl bromides under mild conditions, using water-soluble, sterically demanding alkylphosphines.
    DeVasher RB, Moore LR, Shaughnessy KH.
    J Org Chem; 2004 Nov 12; 69(23):7919-27. PubMed ID: 15527271
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  • 12. Efficient Stille cross-coupling reaction using aryl chlorides or bromides in water.
    Wolf C, Lerebours R.
    J Org Chem; 2003 Sep 19; 68(19):7551-4. PubMed ID: 12968920
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  • 13. P[N(i-Bu)CH2CH2]3N: a versatile ligand for the Pd-catalyzed amination of aryl chlorides.
    Urgaonkar S, Nagarajan M, Verkade JG.
    Org Lett; 2003 Mar 20; 5(6):815-8. PubMed ID: 12633079
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  • 14. Pd2(dba)3/P(i-BuNCH2CH2)3N-catalyzed Stille cross-coupling of aryl chlorides.
    Su W, Urgaonkar S, Verkade JG.
    Org Lett; 2004 Apr 29; 6(9):1421-4. PubMed ID: 15101757
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  • 15. P(i-BuNCH2CH2)3N: an efficient ligand for the direct alpha-arylation of nitriles with aryl bromides.
    You J, Verkade JG.
    J Org Chem; 2003 Oct 17; 68(21):8003-7. PubMed ID: 14535776
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  • 20. An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides.
    Battistuzzi G, Cacchi S, Fabrizi G.
    Org Lett; 2003 Mar 06; 5(5):777-80. PubMed ID: 12605513
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