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Items: 1 to 20 of 99

1.

Gold Catalysed Redox Synthesis of Imidazo[1,2-a]pyridine using Pyridine N-Oxide and Alkynes.

Talbot EP, Richardson M, McKenna JM, Toste FD.

Adv Synth Catal. 2014 Mar 10;356(4):687-691.

2.
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Directed solid-phase synthesis of trisubstituted imidazo[4,5-c]pyridines and imidazo[4,5-b]pyridines.

Lemrová B, Smyslová P, Popa I, Oždian T, Zajdel P, Soural M.

ACS Comb Sci. 2014 Oct 13;16(10):558-65. doi: 10.1021/co500090t. Epub 2014 Jul 31.

PMID:
25046560
4.

General Method for the Preparation of Electron-Deficient Imidazo[1,2-a]pyridines and Related Heterocycles.

McDonald IM, Peese KM.

Org Lett. 2015 Dec 18;17(24):6002-5. doi: 10.1021/acs.orglett.5b02966. Epub 2015 Nov 24.

PMID:
26598965
5.

Pyridine N-Oxide vs Pyridine Substrates for Rh(III)-Catalyzed Oxidative C-H Bond Functionalization.

Neufeldt SR, Jiménez-Osés G, Huckins JR, Thiel OR, Houk KN.

J Am Chem Soc. 2015 Aug 12;137(31):9843-54. doi: 10.1021/jacs.5b03535. Epub 2015 Aug 3.

PMID:
26197041
6.

Efficient solid-phase synthesis of a library of imidazo[1,2-a]pyridine-8-carboxamides.

Kamal A, Devaiah V, Reddy KL, Rajendar, Shetti RV, Shankaraiah N.

J Comb Chem. 2007 Mar-Apr;9(2):267-74. Epub 2007 Feb 24.

PMID:
17319727
7.
8.

Copper(II)-Mediated Aerobic Synthesis of Imidazo[1,2-a]pyridines via Cascade Aminomethylation/Cycloisomerization of Alkynes.

Rassokhina IV, Shirinian VZ, Zavarzin IV, Gevorgyan V, Volkova YA.

J Org Chem. 2015 Nov 6;80(21):11212-8. doi: 10.1021/acs.joc.5b02102. Epub 2015 Oct 21.

PMID:
26457968
9.

Vertically-expanded imidazo[1,2-a]pyridines and imidazo[1,5-a]pyridine via dehydrogenative coupling.

Firmansyah D, Banasiewicz M, Gryko DT.

Org Biomol Chem. 2015 Feb 7;13(5):1367-74. doi: 10.1039/c4ob02383h.

PMID:
25452099
10.

Transition metal-mediated C═O and C═C bond-forming reactions: a regioselective strategy for the synthesis of imidazo[1,2-a]pyridines and imidazo[1,2-a]pyrazines.

Cao H, Liu X, Liao J, Huang J, Qiu H, Chen Q, Chen Y.

J Org Chem. 2014 Nov 21;79(22):11209-14. doi: 10.1021/jo501671x. Epub 2014 Nov 4.

PMID:
25369461
11.

A practical and efficient approach to imidazo[1,2-a]pyridine-fused isoquinolines through the post-GBB transformation strategy.

Shao T, Gong Z, Su T, Hao W, Che C.

Beilstein J Org Chem. 2017 May 4;13:817-824. doi: 10.3762/bjoc.13.82. eCollection 2017.

12.

Four-component cascade heteroannulation of heterocyclic ketene aminals: synthesis of functionalized tetrahydroimidazo[1,2-a]pyridine derivatives.

Li M, Shao P, Wang SW, Kong W, Wen LR.

J Org Chem. 2012 Oct 19;77(20):8956-67. doi: 10.1021/jo3013836. Epub 2012 Sep 26.

PMID:
22970749
13.

Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents.

Ismail MA, Brun R, Wenzler T, Tanious FA, Wilson WD, Boykin DW.

J Med Chem. 2004 Jul 1;47(14):3658-64.

PMID:
15214792
14.

A base promoted cyclization of N-propargylaminopyridines. Synthesis of imidazo[1,2-a]pyridine derivatives.

Husinec S, Markovic R, Petkovic M, Nasufovic V, Savic V.

Org Lett. 2011 May 6;13(9):2286-9. doi: 10.1021/ol200508x. Epub 2011 Mar 29.

PMID:
21446664
15.

Gold-catalysed cycloisomerisation reactions of 2-(2-propynyl)pyridine N-oxides leading to indolizinones.

Murai M, Kitabata S, Okamoto K, Ohe K.

Chem Commun (Camb). 2012 Aug 7;48(61):7622-4. doi: 10.1039/c2cc32628k. Epub 2012 Jun 25.

PMID:
22728547
17.

Synthesis of potential anticancer agents: imidazo[4,5-c]pyridines and imidazo[4,5-b]pyridines.

Temple C Jr, Rose JD, Comber RN, Rener GA.

J Med Chem. 1987 Oct;30(10):1746-51.

PMID:
3656351
18.

One-Pot Cascade Reactions Leading to Pyrido[2',1':2,3]imidazo[4,5-c][1,2,3]triazolo[1,5-a]quinolines under Bimetallic Relay Catalysis with Air as the Oxidant.

Wang Z, Li B, Zhang X, Fan X.

J Org Chem. 2016 Aug 5;81(15):6357-63. doi: 10.1021/acs.joc.6b00996. Epub 2016 Jul 13.

PMID:
27351209
19.

Direct Alkynylation of 3H-Imidazo[4,5-b]pyridines Using gem-Dibromoalkenes as Alkynes Source.

Aziz J, Baladi T, Piguel S.

J Org Chem. 2016 May 20;81(10):4122-33. doi: 10.1021/acs.joc.6b00406. Epub 2016 May 5.

PMID:
27111189
20.

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