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Items: 1 to 20 of 131

1.
2.

Mo-Au combo catalysis for rapid 1,3-rearrangement of propargyl alcohols into alpha,beta-unsaturated carbonyl compounds.

Egi M, Yamaguchi Y, Fujiwara N, Akai S.

Org Lett. 2008 May 1;10(9):1867-70. doi: 10.1021/ol800596c. Epub 2008 Apr 8.

PMID:
18393519
3.

One-pot synthesis of optically active allyl esters via lipase-vanadium combo catalysis.

Akai S, Hanada R, Fujiwara N, Kita Y, Egi M.

Org Lett. 2010 Nov 5;12(21):4900-3. doi: 10.1021/ol102053a.

PMID:
20936813
4.

Synthesis of α-allylated α,β-unsaturated carbonyl compounds using vanadium/palladium contemporaneous dual catalysis.

Trost BM, Luan X.

Nat Protoc. 2012 Jul 12;7(8):1497-501. doi: 10.1038/nprot.2012.076.

PMID:
22790085
5.

Gold- and silver-catalyzed reactions of propargylic alcohols in the presence of protic additives.

Pennell MN, Turner PG, Sheppard TD.

Chemistry. 2012 Apr 10;18(15):4748-58. doi: 10.1002/chem.201102830. Epub 2012 Feb 28.

PMID:
22374879
6.
7.

Regioselectivity switch: gold(I)-catalyzed oxidative rearrangement of propargyl alcohols to 1,3-diketones.

Hashmi AS, Wang T, Shi S, Rudolph M.

J Org Chem. 2012 Sep 7;77(17):7761-7. doi: 10.1021/jo301381z. Epub 2012 Aug 21.

PMID:
22877083
8.

A general procedure for the synthesis of enones via gold-catalyzed Meyer-Schuster rearrangement of propargylic alcohols at room temperature.

Pennell MN, Unthank MG, Turner P, Sheppard TD.

J Org Chem. 2011 Mar 4;76(5):1479-82. doi: 10.1021/jo102263t. Epub 2011 Jan 25.

PMID:
21265538
9.

Heteropoly compound catalyzed synthesis of both Z- and E-α,β-unsaturated carbonyl compounds.

Egi M, Umemura M, Kawai T, Akai S.

Angew Chem Int Ed Engl. 2011 Dec 16;50(51):12197-200. doi: 10.1002/anie.201106381. Epub 2011 Oct 25. No abstract available.

PMID:
22025405
10.

[The chemistry of pericyclic reactions and their application to syntheses of heterocyclic compounds].

Sakamoto M, Kawasaki T, Ishii K, Tamura O.

Yakugaku Zasshi. 2003 Sep;123(9):717-59. Review. Japanese.

11.
12.

Gold mediated glycosylations: selective activation of propargyl 1,2-orthoesters in the presence of aglycones containing a propargyl moiety.

Sureshkumar G, Hotha S.

Chem Commun (Camb). 2008 Sep 28;(36):4282-4. doi: 10.1039/b806707d. Epub 2008 Jul 21.

PMID:
18802544
13.

A simple and versatile re-catalyzed Meyer-Schuster rearrangement of propargylic alcohols to alpha,beta-unsaturated carbonyl compounds.

Stefanoni M, Luparia M, Porta A, Zanoni G, Vidari G.

Chemistry. 2009;15(16):3940-4. doi: 10.1002/chem.200802622.

PMID:
19283809
14.

Heteropolyacid-catalyzed direct deoxygenation of propargyl and allyl alcohols.

Egi M, Kawai T, Umemura M, Akai S.

J Org Chem. 2012 Aug 17;77(16):7092-7. doi: 10.1021/jo300889p. Epub 2012 Aug 9.

PMID:
22849794
15.
16.

Vanadium-catalyzed addition of propargyl alcohols and imines.

Trost BM, Chung CK.

J Am Chem Soc. 2006 Aug 16;128(32):10358-9.

17.

Synthesis of functionalized indenes via cascade reaction of aziridines and propargyl alcohols.

Wang S, Zhu Y, Wang Y, Lu P.

Org Lett. 2009 Jun 18;11(12):2615-8. doi: 10.1021/ol901033h.

PMID:
19449884
18.

Chiral propargyl alcohols via the enantioselective addition of terminal di- and triynes to aldehydes.

Graham ER, Tykwinski RR.

J Org Chem. 2011 Aug 19;76(16):6574-83. doi: 10.1021/jo2008719. Epub 2011 Jul 25.

PMID:
21749074
19.

Iron-catalyzed C-O bond activation for the synthesis of propargyl-1,2,3-triazoles and 1,1-bis-triazoles.

Yan W, Wang Q, Chen Y, Petersen JL, Shi X.

Org Lett. 2010 Aug 6;12(15):3308-11. doi: 10.1021/ol101082v.

PMID:
20617810
20.

Highly chemoselective calcium-catalyzed propargylic deoxygenation.

Meyer VJ, Niggemann M.

Chemistry. 2012 Apr 10;18(15):4687-91. doi: 10.1002/chem.201103691. Epub 2012 Feb 29.

PMID:
22378484

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