Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 82

1.

Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.

Swift EC, Jarvo ER.

Tetrahedron. 2013 Jul 22;69(29):5799-5817. No abstract available.

2.

N-tosylhydrazones: versatile reagents for metal-catalyzed and metal-free cross-coupling reactions.

Shao Z, Zhang H.

Chem Soc Rev. 2012 Jan 21;41(2):560-72. doi: 10.1039/c1cs15127d. Epub 2011 Jul 25. Review.

PMID:
21785803
4.
5.

Diazo compounds and N-tosylhydrazones: novel cross-coupling partners in transition-metal-catalyzed reactions.

Xiao Q, Zhang Y, Wang J.

Acc Chem Res. 2013 Feb 19;46(2):236-47. doi: 10.1021/ar300101k. Epub 2012 Sep 26.

PMID:
23013153
6.

Zirconium-Catalyzed Asymmetric Carboalumination of Unactivated Terminal Alkenes.

Xu S, Negishi EI.

Acc Chem Res. 2016 Oct 18;49(10):2158-2168. Epub 2016 Sep 29.

PMID:
27685327
8.

Chiral diphosphine and monodentate phosphorus ligands on a spiro scaffold for transition-metal-catalyzed asymmetric reactions.

Xie JH, Zhou QL.

Acc Chem Res. 2008 May;41(5):581-93. doi: 10.1021/ar700137z. Epub 2008 Mar 1.

PMID:
18311931
9.

Asymmetric Construction of Functionalized 1,2-Dihydropyridine and Pyridine Derivatives with Adjacent Stereocenters via a Unified Metal-Free Catalytic Approach.

Zou GF, Zhang SQ, Wang JX, Liao WW.

J Org Chem. 2016 Jul 1;81(13):5717-25. doi: 10.1021/acs.joc.6b00791. Epub 2016 Jun 20.

PMID:
27285943
10.

Transition-metal-catalyzed C-N bond forming reactions using organic azides as the nitrogen source: a journey for the mild and versatile C-H amination.

Shin K, Kim H, Chang S.

Acc Chem Res. 2015 Apr 21;48(4):1040-52. doi: 10.1021/acs.accounts.5b00020. Epub 2015 Mar 30.

PMID:
25821998
11.
12.

Transition-metal catalyzed oxidative cross-coupling reactions to form C-C bonds involving organometallic reagents as nucleophiles.

Shi W, Liu C, Lei A.

Chem Soc Rev. 2011 May;40(5):2761-76. doi: 10.1039/c0cs00125b. Epub 2011 Jan 31.

PMID:
21283847
13.

Transition metal-catalyzed cross-coupling reactions using organoindium reagents.

Zhao K, Shen L, Shen ZL, Loh TP.

Chem Soc Rev. 2017 Feb 6;46(3):586-602. doi: 10.1039/c6cs00465b.

PMID:
27827485
14.

Gold(I)-catalyzed enantioselective synthesis of benzopyrans via rearrangement of allylic oxonium intermediates.

Uemura M, Watson ID, Katsukawa M, Toste FD.

J Am Chem Soc. 2009 Mar 18;131(10):3464-5. doi: 10.1021/ja900155x.

15.

Asymmetric hydroxyamination of oxindoles catalyzed by chiral bifunctional tertiary amine thiourea: construction of 3-amino-2-oxindoles with quaternary stereocenters.

Jia LN, Huang J, Peng L, Wang LL, Bai JF, Tian F, He GY, Xu XY, Wang LX.

Org Biomol Chem. 2012 Jan 14;10(2):236-9. doi: 10.1039/c1ob06413d. Epub 2011 Oct 21.

PMID:
22016069
16.

Palladium-catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with Michael acceptors: construction of vicinal quaternary stereocenters.

Khan A, Yang L, Xu J, Jin LY, Zhang YJ.

Angew Chem Int Ed Engl. 2014 Oct 13;53(42):11257-60. doi: 10.1002/anie.201407013. Epub 2014 Aug 28. Erratum in: Angew Chem Int Ed Engl. 2015 Jul 20;54(30):8584.

PMID:
25168969
18.
19.

Secondary alkyl halides in transition-metal-catalyzed cross-coupling reactions.

Rudolph A, Lautens M.

Angew Chem Int Ed Engl. 2009;48(15):2656-70. doi: 10.1002/anie.200803611. Review.

PMID:
19173365
20.

Functional-group-tolerant, nickel-catalyzed cross-coupling reaction for enantioselective construction of tertiary methyl-bearing stereocenters.

Wisniewska HM, Swift EC, Jarvo ER.

J Am Chem Soc. 2013 Jun 19;135(24):9083-90. doi: 10.1021/ja4034999. Epub 2013 Jun 10.

Supplemental Content

Support Center