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Items: 1 to 20 of 110

1.

Catalyst-controlled C-O versus C-N allylic functionalization of terminal olefins.

Strambeanu II, White MC.

J Am Chem Soc. 2013 Aug 14;135(32):12032-7. doi: 10.1021/ja405394v. Epub 2013 Jul 31.

2.

N-Boc amines to oxazolidinones via Pd(II)/bis-sulfoxide/Brønsted acid co-catalyzed allylic C-H oxidation.

Osberger TJ, White MC.

J Am Chem Soc. 2014 Aug 6;136(31):11176-81. doi: 10.1021/ja506036q. Epub 2014 Jul 24.

3.
4.

Allylic C-H amination for the preparation of syn-1,3-amino alcohol motifs.

Rice GT, White MC.

J Am Chem Soc. 2009 Aug 26;131(33):11707-11. doi: 10.1021/ja9054959.

5.

Catalytic enantioselective allylic amination of unactivated terminal olefins via an ene reaction/[2,3]-rearrangement.

Bao H, Tambar UK.

J Am Chem Soc. 2012 Nov 14;134(45):18495-8. doi: 10.1021/ja307851b. Epub 2012 Oct 29.

6.

syn-1,2-Amino alcohols via diastereoselective allylic C-H amination.

Fraunhoffer KJ, White MC.

J Am Chem Soc. 2007 Jun 13;129(23):7274-6. Epub 2007 May 22. No abstract available.

7.

Terminal olefins to chromans, isochromans, and pyrans via allylic C-H oxidation.

Ammann SE, Rice GT, White MC.

J Am Chem Soc. 2014 Aug 6;136(31):10834-7. doi: 10.1021/ja503322e. Epub 2014 Jul 16.

8.

Enantioselective functionalization of allylic C-H bonds following a strategy of functionalization and diversification.

Sharma A, Hartwig JF.

J Am Chem Soc. 2013 Nov 27;135(47):17983-9. doi: 10.1021/ja409995w. Epub 2013 Nov 14.

9.

Palladium-catalyzed asymmetric allylic amination of racemic butadiene monoxide with isatin derivatives.

Li G, Feng X, Du H.

Org Biomol Chem. 2015 May 28;13(20):5826-30. doi: 10.1039/c5ob00663e. Epub 2015 Apr 28.

PMID:
25917274
10.

Palladium-catalyzed allylic C-H amination of alkenes with N-fluorodibenzenesulfonimide: water plays an important role.

Xiong T, Li Y, Mao L, Zhang Q, Zhang Q.

Chem Commun (Camb). 2012 Feb 21;48(16):2246-8. doi: 10.1039/c2cc16720d. Epub 2012 Jan 17.

PMID:
22252277
11.

The synthesis of chiral β-aryl-α,β-unsaturated amino alcohols via a Pd-catalyzed asymmetric allylic amination.

Quan M, Butt N, Shen J, Shen K, Liu D, Zhang W.

Org Biomol Chem. 2013 Nov 14;11(42):7412-9. doi: 10.1039/c3ob41642a.

PMID:
24077558
12.

Catalytic diamination of olefins via N-N bond activation.

Zhu Y, Cornwall RG, Du H, Zhao B, Shi Y.

Acc Chem Res. 2014 Dec 16;47(12):3665-78. doi: 10.1021/ar500344t. Epub 2014 Nov 17.

13.

Palladium-catalyzed sequential one-pot reaction of aryl bromides with O-homoallylhydroxylamines: synthesis of N-aryl-beta-amino alcohols.

Peng J, Jiang D, Lin W, Chen Y.

Org Biomol Chem. 2007 May 7;5(9):1391-6. Epub 2007 Mar 21.

PMID:
17464408
14.

Pd(II)-catalyzed allylic C-H amination for the preparation of 1,2- and 1,3-cyclic ureas.

Nishikawa Y, Kimura S, Kato Y, Yamazaki N, Hara O.

Org Lett. 2015 Feb 20;17(4):888-91. doi: 10.1021/ol5037453. Epub 2015 Jan 30.

PMID:
25632830
15.

Catalytic intermolecular allylic C-H alkylation.

Young AJ, White MC.

J Am Chem Soc. 2008 Oct 29;130(43):14090-1. doi: 10.1021/ja806867p. Epub 2008 Oct 3.

PMID:
18831588
16.

Activation of allylic C-F bonds: palladium-catalyzed allylic amination of 3,3-difluoropropenes.

Pigeon X, Bergeron M, Barabé F, Dubé P, Frost HN, Paquin JF.

Angew Chem Int Ed Engl. 2010 Feb 1;49(6):1123-7. doi: 10.1002/anie.200904747. No abstract available.

PMID:
20043303
17.

In situ generated bulky palladium hydride complexes as catalysts for the efficient isomerization of olefins. Selective transformation of terminal alkenes to 2-alkenes.

Gauthier D, Lindhardt AT, Olsen EP, Overgaard J, Skrydstrup T.

J Am Chem Soc. 2010 Jun 16;132(23):7998-8009. doi: 10.1021/ja9108424.

PMID:
20481527
18.
19.

Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols.

Deng Z, Wei J, Liao L, Huang H, Zhao X.

Org Lett. 2015 Apr 17;17(8):1834-7. doi: 10.1021/acs.orglett.5b00213. Epub 2015 Apr 7.

PMID:
25849818
20.

Palladium nanoparticle-catalyzed C-N bond formation. A highly regio- and stereoselective allylic amination by allyl acetates.

Adak L, Chattopadhyay K, Ranu BC.

J Org Chem. 2009 May 15;74(10):3982-5. doi: 10.1021/jo9003037.

PMID:
19382763

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