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Items: 1 to 20 of 113

1.

A simple, multidimensional approach to high-throughput discovery of catalytic reactions.

Robbins DW, Hartwig JF.

Science. 2011 Sep 9;333(6048):1423-7. doi: 10.1126/science.1207922.

2.

Chemistry. High-throughput discovery of new chemical reactions.

Montgomery J.

Science. 2011 Sep 9;333(6048):1387-8. doi: 10.1126/science.1210735. No abstract available.

PMID:
21903798
3.

Cycloaddition reactivity studies of first-row transition metal-azide complexes and alkynes: an inorganic click reaction for metalloenzyme inhibitor synthesis.

Evangelio E, Rath NP, Mirica LM.

Dalton Trans. 2012 Jul 14;41(26):8010-21. doi: 10.1039/c2dt30145h. Epub 2012 Apr 20.

PMID:
22517535
4.

More than bystanders: the effect of olefins on transition-metal-catalyzed cross-coupling reactions.

Johnson JB, Rovis T.

Angew Chem Int Ed Engl. 2008;47(5):840-71. Review.

PMID:
18081111
5.

Catalysis with complexes containing stereogenic metal centers.

Kündig EP.

Chimia (Aarau). 2014;68(5):312-4. doi: 10.2533/chimia.2014.312.

PMID:
24983806
6.

Transition metal-carboryne complexes: synthesis, bonding, and reactivity.

Qiu Z, Ren S, Xie Z.

Acc Chem Res. 2011 Apr 19;44(4):299-309. doi: 10.1021/ar100156f. Epub 2011 Mar 11. Review.

PMID:
21395260
7.

All kinds of reactivity: recent breakthroughs in metal-catalyzed alkyne chemistry.

Anaya de Parrodi C, Walsh PJ.

Angew Chem Int Ed Engl. 2009;48(26):4679-82. doi: 10.1002/anie.200900900.

8.

Well-defined diimine copper(I) complexes as catalysts in click azide-alkyne cycloaddition reactions.

Barta JM, Díez-González S.

Molecules. 2013 Jul 26;18(8):8919-28. doi: 10.3390/molecules18088919.

9.

Mechanistic Basis for Regioselection and Regiodivergence in Nickel-Catalyzed Reductive Couplings.

Jackson EP, Malik HA, Sormunen GJ, Baxter RD, Liu P, Wang H, Shareef AR, Montgomery J.

Acc Chem Res. 2015 Jun 16;48(6):1736-45. doi: 10.1021/acs.accounts.5b00096. Epub 2015 May 12.

10.

Synthesis of [3]Rotaxanes by the Combination of Copper-Mediated Coupling Reaction and Metal-Template Approach.

Hayashi R, Mutoh Y, Kasama T, Saito S.

J Org Chem. 2015 Aug 7;80(15):7536-46. doi: 10.1021/acs.joc.5b01120. Epub 2015 Jul 24.

PMID:
26161508
11.

Combinatorial libraries of transition-metal complexes, catalysts and materials.

Francis MB, Jamison TF, Jacobsen EN.

Curr Opin Chem Biol. 1998 Jun;2(3):422-8. Review.

PMID:
9691076
12.

Synthesis of heterocycles via transition-metal-catalyzed hydroarylation of alkynes.

Yamamoto Y.

Chem Soc Rev. 2014 Mar 7;43(5):1575-600. doi: 10.1039/c3cs60369e. Epub 2013 Dec 16. Review.

PMID:
24336638
13.
14.

Nickel-catalyzed sonogashira reactions of non-activated secondary alkyl bromides and iodides.

Yi J, Lu X, Sun YY, Xiao B, Liu L.

Angew Chem Int Ed Engl. 2013 Nov 18;52(47):12409-13. doi: 10.1002/anie.201307069. Epub 2013 Oct 2.

PMID:
24115611
15.

Hydroamination of terminal alkynes with secondary amines catalyzed by copper: regioselective access to amines.

Bahri J, Blieck R, Jamoussi B, Taillefer M, Monnier F.

Chem Commun (Camb). 2015 Jun 30;51(56):11210-2. doi: 10.1039/c5cc02677f.

PMID:
26077650
16.

Hydroarylation of alkynes catalyzed by nickel.

Nakao Y.

Chem Rec. 2011 Sep;11(5):242-51. doi: 10.1002/tcr.201100023. Epub 2011 Sep 6. Review.

PMID:
21898779
17.

Non-precious metals catalyze formal [4 + 2] cycloaddition reactions of 1,2-diazines and siloxyalkynes under ambient conditions.

Sumaria CS, Türkmen YE, Rawal VH.

Org Lett. 2014 Jun 20;16(12):3236-9. doi: 10.1021/ol501254h. Epub 2014 Jun 9.

18.

Cu-catalyzed formal methylative and hydrogenative carboxylation of alkynes with carbon dioxide: efficient synthesis of α,β-unsaturated carboxylic acids.

Takimoto M, Hou Z.

Chemistry. 2013 Aug 19;19(34):11439-45. doi: 10.1002/chem.201301456. Epub 2013 Jul 12.

PMID:
23852827
20.

Consecutive intermolecular reductive hydroamination: cooperative transition-metal and chiral Brønsted acid catalysis.

Fleischer S, Werkmeister S, Zhou S, Junge K, Beller M.

Chemistry. 2012 Jul 16;18(29):9005-10. doi: 10.1002/chem.201200109. Epub 2012 Jun 15.

PMID:
22707210

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