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Results: 1 to 20 of 186

Similar articles for PubMed (Select 24533440)

1.

Melamine and melamine-formaldehyde polymers as ligands for palladium and application to Suzuki-Miyaura cross-coupling reactions in sustainable solvents.

Edwards GA, Trafford MA, Hamilton AE, Buxton AM, Bardeaux MC, Chalker JM.

J Org Chem. 2014 Mar 7;79(5):2094-104. doi: 10.1021/jo402799t. Epub 2014 Feb 17.

PMID:
24533440
2.

Suzuki-Miyaura cross-coupling coupling reactions with low catalyst loading: a green and sustainable protocol in pure water.

Fihri A, Luart D, Len C, Solhy A, Chevrin C, Polshettiwar V.

Dalton Trans. 2011 Apr 7;40(13):3116-21. doi: 10.1039/c0dt01637c. Epub 2011 Feb 22.

PMID:
21340087
3.

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.

Martin R, Buchwald SL.

Acc Chem Res. 2008 Nov 18;41(11):1461-73. doi: 10.1021/ar800036s.

4.

Suzuki-Miyaura cross-coupling reactions in aqueous media: green and sustainable syntheses of biaryls.

Polshettiwar V, Decottignies A, Len C, Fihri A.

ChemSusChem. 2010 May 25;3(5):502-22. doi: 10.1002/cssc.200900221. Review.

PMID:
20191633
5.

"Homeopathic" palladium nanoparticle catalysis of cross carbon-carbon coupling reactions.

Deraedt C, Astruc D.

Acc Chem Res. 2014 Feb 18;47(2):494-503. doi: 10.1021/ar400168s. Epub 2013 Nov 11.

PMID:
24215156
6.

[Development of novel solid-phase polymeric catalysts for organic syntheses].

Yamada YM.

Yakugaku Zasshi. 2005 Oct;125(10):749-70. Review. Japanese.

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9.

A convenient catalyst for aqueous and protein Suzuki-Miyaura cross-coupling.

Chalker JM, Wood CS, Davis BG.

J Am Chem Soc. 2009 Nov 18;131(45):16346-7. doi: 10.1021/ja907150m.

PMID:
19852502
10.

An expeditious aqueous Suzuki-Miyaura method for the substituted aryl heterocyclics.

Zhang Z, Hu Z, Wang S, Lei P, Chi H, He R.

J Environ Sci (China). 2009;21 Suppl 1:S65-8. doi: 10.1016/S1001-0742(09)60039-5.

PMID:
25084435
11.

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
12.
13.

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
15.
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.

17.

Highly dispersed pd catalyst locked in knitting aryl network polymers for Suzuki-Miyaura coupling reactions of aryl chlorides in aqueous media.

Li B, Guan Z, Wang W, Yang X, Hu J, Tan B, Li T.

Adv Mater. 2012 Jul 3;24(25):3390-5. doi: 10.1002/adma.201200804. Epub 2012 Jun 4.

PMID:
22674537
18.

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
19.

Organosulphur and related ligands in Suzuki-Miyaura C-C coupling.

Kumar A, Rao GK, Kumar S, Singh AK.

Dalton Trans. 2013 Apr 21;42(15):5200-23. doi: 10.1039/c2dt32432f. Epub 2013 Jan 23.

PMID:
23340712
20.
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