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Items: 1 to 20 of 113

1.

Surfactant-free synthesis of palladium nanoclusters for their use in catalytic cross-coupling reactions.

Hyotanishi M, Isomura Y, Yamamoto H, Kawasaki H, Obora Y.

Chem Commun (Camb). 2011 May 28;47(20):5750-2. doi: 10.1039/c1cc11487e. Epub 2011 Apr 18.

PMID:
21503284
2.

Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions.

Marion N, Nolan SP.

Acc Chem Res. 2008 Nov 18;41(11):1440-9. doi: 10.1021/ar800020y.

PMID:
18774825
3.
4.

Recyclable and reusable Pd(OAc)2/DABCO/PEG-400 system for Suzuki-Miyaura cross-coupling reaction.

Li JH, Liu WJ, Xie YX.

J Org Chem. 2005 Jul 8;70(14):5409-12.

PMID:
15989320
5.

Mono- and binuclear cyclometallated palladium(II) complexes containing bridging (N,O-) and terminal (N-) imidate ligands: air stable, thermally robust and recyclable catalysts for cross-coupling processes.

Fairlamb IJ, Kapdi AR, Lee AF, Sánchez G, López G, Serrano JL, García L, Pérez J, Pérez E.

Dalton Trans. 2004 Dec 7;(23):3970-81. Epub 2004 Oct 27.

PMID:
15558122
6.

Practical preparation method of polymer-incarcerated (PI) palladium catalysts using Pd(II) salts.

Hagio H, Sugiura M, Kobayashi S.

Org Lett. 2006 Feb 2;8(3):375-8.

PMID:
16435838
7.

Palladium nanoclusters supported on propylurea-modified siliceous mesocellular foam for coupling and hydrogenation reactions.

Erathodiyil N, Ooi S, Seayad AM, Han Y, Lee SS, Ying JY.

Chemistry. 2008;14(10):3118-25. doi: 10.1002/chem.200701361.

PMID:
18260070
8.

Expanded ring N-heterocyclic carbenes: a comparative study of ring size in palladium (0) catalysed Mizoroki-Heck coupling.

Dunsford JJ, Cavell KJ.

Dalton Trans. 2011 Sep 28;40(36):9131-5. doi: 10.1039/c1dt10596e. Epub 2011 Aug 5.

PMID:
21818498
9.

Simple synthesis of Pd-Fe3O4 heterodimer nanocrystals and their application as a magnetically recyclable catalyst for Suzuki cross-coupling reactions.

Jang Y, Chung J, Kim S, Jun SW, Kim BH, Lee DW, Kim BM, Hyeon T.

Phys Chem Chem Phys. 2011 Feb 21;13(7):2512-6. doi: 10.1039/c0cp01680b. Epub 2011 Jan 4.

PMID:
21203638
10.

Synthesis of a cyclometalated 1,3,5-triphenylpyrazole palladium dimer and its activity towards cross coupling reactions.

Mamidala R, Mukundam V, Dhanunjayarao K, Venkatasubbaiah K.

Dalton Trans. 2015 Mar 28;44(12):5805-9. doi: 10.1039/c4dt03908d.

PMID:
25714046
12.

Spatially controlled Suzuki and Heck catalytic molecular coupling.

Davis JJ, Bagshaw CB, Busuttil KL, Hanyu Y, Coleman KS.

J Am Chem Soc. 2006 Nov 1;128(43):14135-41.

PMID:
17061897
13.

Supported synthesis and functionnalization of 2''-deoxyuridine by Suzuki-Miyaura cross-coupling.

El Kazzouli S, Berteina-Raboin S, Agrofoglio LA.

Nucleosides Nucleotides Nucleic Acids. 2007;26(10-12):1395-8.

PMID:
18066790
14.

Palladium(II) complexes based on 1,8-naphthyridine functionalized N-heterocyclic carbenes (NHC) and their catalytic activity.

Chang YH, Liu ZY, Liu YH, Peng SM, Chen JT, Liu ST.

Dalton Trans. 2011 Jan 14;40(2):489-94. doi: 10.1039/c0dt00990c. Epub 2010 Nov 26.

PMID:
21113540
15.

Heterogeneous Pd/C-catalyzed ligand-free, room-temperature Suzuki-Miyaura coupling reactions in aqueous media.

Maegawa T, Kitamura Y, Sako S, Udzu T, Sakurai A, Tanaka A, Kobayashi Y, Endo K, Bora U, Kurita T, Kozaki A, Monguchi Y, Sajiki H.

Chemistry. 2007;13(20):5937-43.

PMID:
17444548
16.

Palladium(0) deposited on PAMAM dendrimers as a catalyst for C-C cross coupling reactions.

Borkowski T, Subik P, Trzeciak AM, Wołowiec S.

Molecules. 2011 Jan 10;16(1):427-41. doi: 10.3390/molecules16010427.

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