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Items: 1 to 20 of 112

1.

An active, general, and long-lived palladium catalyst for cross-couplings of deactivated (hetero)aryl chlorides and bromides with arylboronic acids.

Hoshi T, Honma T, Mori A, Konishi M, Sato T, Hagiwara H, Suzuki T.

J Org Chem. 2013 Nov 15;78(22):11513-24. doi: 10.1021/jo402089r. Epub 2013 Nov 7.

PMID:
24161157
2.

Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of sterically hindered aryl bromides.

Hoshi T, Saitoh I, Nakazawa T, Suzuki T, Sakai J, Hagiwara H.

J Org Chem. 2009 May 15;74(10):4013-6. doi: 10.1021/jo900550g.

PMID:
19391580
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Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of aryl chlorides.

Hoshi T, Nakazawa T, Saitoh I, Mori A, Suzuki T, Sakai J, Hagiwara H.

Org Lett. 2008 May 15;10(10):2063-6. doi: 10.1021/ol800567q. Epub 2008 Apr 19.

PMID:
18422322
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Simple palladium(II) precatalyst for Suzuki-Miyaura couplings: efficient reactions of benzylic, aryl, heteroaryl, and vinyl coupling partners.

Burns MJ, Fairlamb IJ, Kapdi AR, Sehnal P, Taylor RJ.

Org Lett. 2007 Dec 20;9(26):5397-400. Epub 2007 Nov 30.

PMID:
18047357
11.

A general and efficient catalyst for palladium-catalyzed C-O coupling reactions of aryl halides with primary alcohols.

Gowrisankar S, Sergeev AG, Anbarasan P, Spannenberg A, Neumann H, Beller M.

J Am Chem Soc. 2010 Aug 25;132(33):11592-8. doi: 10.1021/ja103248d.

PMID:
20672810
12.

[2.2]Paracyclophane-based monophosphine ligand for palladium-catalyzed cross-coupling reactions of aryl chlorides.

Ruan J, Shearer L, Mo J, Bacsa J, Zanotti-Gerosa A, Hancock F, Wu X, Xiao J.

Org Biomol Chem. 2009 Aug 21;7(16):3236-42. doi: 10.1039/b906139h. Epub 2009 Jun 17.

PMID:
19641780
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A highly active catalytic system for Suzuki-Miyaura cross-coupling reactions of aryl and heteroaryl chlorides in water.

Mao SL, Sun Y, Yu GA, Zhao C, Han ZJ, Yuan J, Zhu X, Yang Q, Liu SH.

Org Biomol Chem. 2012 Dec 21;10(47):9410-7. doi: 10.1039/c2ob26463c. Epub 2012 Oct 30.

PMID:
23111458
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(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. doi: 10.1021/jo702367k. Epub 2008 Mar 28.

PMID:
18370424
17.

Catalytic sequential reactions involving palladacycle-directed aryl coupling steps.

Catellani M, Motti E, Della Ca' N.

Acc Chem Res. 2008 Nov 18;41(11):1512-22. doi: 10.1021/ar800040u.

PMID:
18680317
18.

Convenient and efficient Suzuki-Miyaura cross-coupling catalyzed by a palladium/diazabutadiene system.

Grasa GA, Hillier AC, Nolan SP.

Org Lett. 2001 Apr 5;3(7):1077-80.

PMID:
11277799
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