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Items: 1 to 20 of 98

1.

The Pauson-Khand mechanism revisited: origin of CO in the final product.

Lesage D, Milet A, Memboeuf A, Blu J, Greene AE, Tabet JC, Gimbert Y.

Angew Chem Int Ed Engl. 2014 Feb 10;53(7):1939-42. doi: 10.1002/anie.201307745. Epub 2014 Jan 21.

PMID:
24449220
2.
3.

The Pauson-Khand reaction: the catalytic age is here!

Gibson SE, Stevenazzi A.

Angew Chem Int Ed Engl. 2003 Apr 25;42(16):1800-10.

PMID:
12722067
4.

Density functional studies on the Pauson--Khand reaction.

Yamanaka M, Nakamura E.

J Am Chem Soc. 2001 Feb 28;123(8):1703-8.

PMID:
11456770
6.
7.

Advances in the Pauson-Khand reaction: development of reactive cobalt complexes.

Sugihara T, Yamaguchi M, Nishizawa M.

Chemistry. 2001 Apr 17;7(8):1589-95.

PMID:
11349898
8.

On the mechanism of the palladium catalyzed intramolecular Pauson-Khand-type reaction.

Lan Y, Deng L, Liu J, Wang C, Wiest O, Yang Z, Wu YD.

J Org Chem. 2009 Jul 17;74(14):5049-58. doi: 10.1021/jo900919v.

PMID:
19469502
9.
10.

The intermolecular Pauson-Khand reaction.

Gibson SE, Mainolfi N.

Angew Chem Int Ed Engl. 2005 May 13;44(20):3022-37. Review.

PMID:
15800868
11.

CO-transfer carbonylation reactions. A catalytic Pauson-Khand-type reaction of enynes with aldehydes as a source of carbon monoxide.

Morimoto T, Fuji K, Tsutsumi K, Kakiuchi K.

J Am Chem Soc. 2002 Apr 17;124(15):3806-7.

PMID:
11942798
12.

Insight into the reactivity of olefins in the Pauson-Khand reaction.

de Bruin TJ, Milet A, Greene AE, Gimbert Y.

J Org Chem. 2004 Feb 20;69(4):1075-80.

PMID:
14961654
13.

Synthesis of tricyclic aromatic compounds by the intramolecular pauson-khand reaction promoted by molecular sieves(,)(1)

Perez-Serrano L, Blanco-Urgoiti J, Casarrubios L, Dominguez G, Perez-Castells J.

J Org Chem. 2000 Jun 2;65(11):3513-9.

PMID:
10843639
15.

On early events in the Pauson-Khand reaction.

Gimbert Y, Lesage D, Milet A, Fournier F, Greene AE, Tabet JC.

Org Lett. 2003 Oct 30;5(22):4073-5.

PMID:
14572252
16.

Cobalt/rhodium heterobimetallic nanoparticle-catalyzed carbonylative [2+2+1] cycloaddition of allenes and bisallenes to Pauson-Khand-type reaction products.

Park JH, Kim E, Kim HM, Choi SY, Chung YK.

Chem Commun (Camb). 2008 May 28;(20):2388-90. doi: 10.1039/b718107h. Epub 2008 Apr 11.

PMID:
18473079
17.
18.

Phosphane Sulfide/Octacarbonyldicobalt-Catalyzed Pauson - Khand Reaction Under an Atmospheric Pressure of Carbon Monoxide.

Hayashi M, Hashimoto Y, Yamamoto Y, Usuki J, Saigo K.

Angew Chem Int Ed Engl. 2000 Feb;39(3):631-633.

PMID:
10671281
20.

Low-energy pathway for pauson-khand reactions: synthesis and reactivity of dicobalt hexacarbonyl complexes of chiral ynamines

Balsells J, Vazquez J, Moyano A, Pericas MA, Riera A.

J Org Chem. 2000 Nov 3;65(22):7291-302.

PMID:
11076586

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