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Items: 1 to 20 of 111

1.

Unexpected E-stereoselective reductive A3-coupling reaction of terminal alkynes with aldehydes and amines.

Fan W, Yuan W, Ma S.

Nat Commun. 2014 May 22;5:3884. doi: 10.1038/ncomms4884.

PMID:
24848772
2.

Copper(I)-catalyzed three-component reaction of terminal propargyl alcohols, aldehydes, and amines: synthesis of 3-amino-2-pyrones and 2,5-dihydrofurans.

Fan W, Ma S.

Angew Chem Int Ed Engl. 2014 Dec 22;53(52):14542-5. doi: 10.1002/anie.201408826. Epub 2014 Oct 29.

PMID:
25353157
3.

Titanium-mediated reductive cross-coupling reactions of imines with terminal alkynes: An efficient route for the synthesis of stereodefined allylic amines.

Mao K, Fan G, Liu Y, Li S, You X, Liu D.

Beilstein J Org Chem. 2013 Mar 27;9:621-7. doi: 10.3762/bjoc.9.69. Print 2013.

4.

Zinc(II)-catalyzed redox cross-dehydrogenative coupling of propargylic amines and terminal alkynes for synthesis of N-tethered 1,6-enynes.

Sugiishi T, Nakamura H.

J Am Chem Soc. 2012 Feb 8;134(5):2504-7. doi: 10.1021/ja211092q. Epub 2012 Jan 30.

PMID:
22283631
5.

Indium-catalyzed highly efficient three-component coupling of aldehyde, alkyne, and amine via C-H bond activation.

Zhang Y, Li P, Wang M, Wang L.

J Org Chem. 2009 Jun 5;74(11):4364-7. doi: 10.1021/jo900507v.

PMID:
19422248
6.

One-pot synthesis of 1,3-disubstituted allenes from 1-alkynes, aldehydes, and morpholine.

Kuang J, Ma S.

J Am Chem Soc. 2010 Feb 17;132(6):1786-7. doi: 10.1021/ja910503k.

PMID:
20102215
7.

Synthesis of mono- and 1,3-disubstituted allenes from propargylic amines via palladium-catalysed hydride-transfer reaction.

Nakamura H, Ishikura M, Sugiishi T, Kamakura T, Biellmann JF.

Org Biomol Chem. 2008 Apr 21;6(8):1471-7. doi: 10.1039/b718298h. Epub 2008 Mar 6.

PMID:
18385854
8.

Protecting-group-free synthesis of amines: synthesis of primary amines from aldehydes via reductive amination.

Dangerfield EM, Plunkett CH, Win-Mason AL, Stocker BL, Timmer MS.

J Org Chem. 2010 Aug 20;75(16):5470-7. doi: 10.1021/jo100004c.

PMID:
20666449
9.

Identifying a Highly Active Copper Catalyst for KA(2) Reaction of Aromatic Ketones.

Cai Y, Tang X, Ma S.

Chemistry. 2016 Feb;22(7):2266-9. doi: 10.1002/chem.201504823. Epub 2016 Jan 12.

PMID:
26660459
10.
11.

An easily removable stereo-dictating group for enantioselective synthesis of propargylic amines.

Fan W, Ma S.

Chem Commun (Camb). 2013 Oct 3;49(86):10175-7. doi: 10.1039/c3cc45118f.

PMID:
24051867
12.

Copper-catalyzed enantioselective propargylic amination of propargylic esters with amines: copper-allenylidene complexes as key intermediates.

Hattori G, Sakata K, Matsuzawa H, Tanabe Y, Miyake Y, Nishibayashi Y.

J Am Chem Soc. 2010 Aug 4;132(30):10592-608. doi: 10.1021/ja1047494.

PMID:
20617844
13.

Highly selective catalytic intermolecular reductive coupling of alkynes and aldehydes

Huang WS, Chan J, Jamison TF.

Org Lett. 2000 Dec 28;2(26):4221-3.

PMID:
11150204
14.

Synthesis of 1,3-Amino Alcohols, 1,3-Diols, Amines, and Carboxylic Acids from Terminal Alkynes.

Zeng M, Herzon SB.

J Org Chem. 2015 Sep 4;80(17):8604-18. doi: 10.1021/acs.joc.5b01220. Epub 2015 Aug 18.

PMID:
26203776
16.

Regioselective Reductive Cross-Coupling Reactions of Unsymmetrical Alkynes.

Reichard HA, McLaughlin M, Chen MZ, Micalizio GC.

European J Org Chem. 2010 Jan;2010(3):391-409.

17.

Highly efficient and diastereoselective gold(I)-catalyzed synthesis of tertiary amines from secondary amines and alkynes: substrate scope and mechanistic insights.

Liu XY, Guo Z, Dong SS, Li XH, Che CM.

Chemistry. 2011 Nov 11;17(46):12932-45. doi: 10.1002/chem.201101982. Epub 2011 Oct 20.

PMID:
22012740
19.

Site-specific modification of amino acids and peptides by aldehyde-alkyne-amine coupling under ambient aqueous conditions.

Uhlig N, Li CJ.

Org Lett. 2012 Jun 15;14(12):3000-3. doi: 10.1021/ol301017q. Epub 2012 May 30.

PMID:
22646971
20.
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