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Items: 1 to 20 of 273

1.

Organocatalytic claisen rearrangement: theory and experiment.

Kirsten M, Rehbein J, Hiersemann M, Strassner T.

J Org Chem. 2007 May 25;72(11):4001-11.

PMID:
17477575
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Catalytic asymmetric Claisen rearrangement of unactivated allyl vinyl ethers.

Geherty ME, Dura RD, Nelson SG.

J Am Chem Soc. 2010 Sep 1;132(34):11875-7. doi: 10.1021/ja1039314.

PMID:
20687554
5.

Tandem Pd(II)-catalyzed vinyl ether exchange-Claisen rearrangement as a facile approach to gamma,delta-unsaturated aldehydes.

Wei X, Lorenz JC, Kapadia S, Saha A, Haddad N, Busacca CA, Senanayake CH.

J Org Chem. 2007 May 25;72(11):4250-3.

PMID:
17447813
7.

Enantioselective Claisen rearrangements with a hydrogen-bond donor catalyst.

Uyeda C, Jacobsen EN.

J Am Chem Soc. 2008 Jul 23;130(29):9228-9. doi: 10.1021/ja803370x.

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Carbanion-accelerated Claisen rearrangements: asymmetric induction with chiral phosphorus-stabilized anions.

Denmark SE, Marlin JE, Rajendra G.

J Org Chem. 2013 Jan 4;78(1):66-82. doi: 10.1021/jo301919e.

10.

Stereoselective synthesis of vinylsilanes by a gold(I)-catalyzed acetylenic sila-cope rearrangement.

Horino Y, Luzung MR, Toste FD.

J Am Chem Soc. 2006 Sep 6;128(35):11364-5.

PMID:
16939254
11.
12.

Brønsted acid catalyzed Morita-Baylis-Hillman reaction: a new mechanistic view for thioureas revealed by ESI-MS(/MS) monitoring and DFT calculations.

Amarante GW, Benassi M, Milagre HM, Braga AA, Maseras F, Eberlin MN, Coelho F.

Chemistry. 2009 Nov 16;15(45):12460-9. doi: 10.1002/chem.200900966.

PMID:
19813234
13.

Halo-enediynes: probing the electronic and stereoelectronic contributions to the Bergman cycloaromatization.

Plourde GW 2nd, Warner PM, Parrish DA, Jones GB.

J Org Chem. 2002 Jul 26;67(15):5369-74.

PMID:
12126430
14.

Gosteli-Claisen rearrangement: substrate synthesis, simple diastereoselectivity, and kinetic studies.

Rehbein J, Leick S, Hiersemann M.

J Org Chem. 2009 Feb 20;74(4):1531-40. doi: 10.1021/jo802303m.

PMID:
19152265
15.

Gold(I)-catalyzed Claisen rearrangement of allenyl vinyl ethers; synthesis of substituted 1,3-dienes.

Krafft ME, Hallal KM, Vidhani DV, Cran JW.

Org Biomol Chem. 2011 Nov 7;9(21):7535-8. doi: 10.1039/c1ob06297b.

PMID:
21938297
16.

Biomimetic trifunctional organocatalyst showing a great acceleration for the transesterification between vinyl ester and alcohol.

Ema T, Tanida D, Matsukawa T, Sakai T.

Chem Commun (Camb). 2008 Feb 28;(8):957-9. doi: 10.1039/b718763g.

PMID:
18283348
17.

One-pot synthesis of 1,2-dihydropyridines: expanding the diverse reactivity of propargyl vinyl ethers.

Harschneck T, Kirsch SF.

J Org Chem. 2011 Apr 1;76(7):2145-56. doi: 10.1021/jo102545m.

PMID:
21381702
18.

A domino copper-catalyzed C-O coupling-Claisen rearrangement process.

Nordmann G, Buchwald SL.

J Am Chem Soc. 2003 Apr 30;125(17):4978-9.

PMID:
12708838
19.

Effect of Lewis acid catalysts on Diels-Alder and hetero-Diels-Alder cycloadditions sharing a common transition state.

Celebi-Olçüm N, Ess DH, Aviyente V, Houk KN.

J Org Chem. 2008 Oct 3;73(19):7472-80. doi: 10.1021/jo801076t.

PMID:
18781801
20.

Mechanistic studies on Au(I)-catalyzed [3,3]-sigmatropic rearrangements using cyclopropane probes.

Mauleón P, Krinsky JL, Toste FD.

J Am Chem Soc. 2009 Apr 1;131(12):4513-20. doi: 10.1021/ja900456m.

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