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Items: 1 to 20 of 151

1.

Tuning the reactivity of TEMPO by coordination to a Lewis acid: isolation and reactivity of MCl3(η1-TEMPO) (M = Fe, Al).

Scepaniak JJ, Wright AM, Lewis RA, Wu G, Hayton TW.

J Am Chem Soc. 2012 Nov 28;134(47):19350-3. doi: 10.1021/ja309499h. Epub 2012 Nov 14.

PMID:
23134421
3.
4.
5.

SBA-15-functionalized TEMPO confined ionic liquid: an efficient catalyst system for transition-metal-free aerobic oxidation of alcohols with improved selectivity.

Karimi B, Badreh E.

Org Biomol Chem. 2011 Jun 7;9(11):4194-8. doi: 10.1039/c1ob05178d. Epub 2011 Apr 20.

PMID:
21505706
6.

Cu-NHC-TEMPO catalyzed aerobic oxidation of primary alcohols to aldehydes.

Liu X, Xia Q, Zhang Y, Chen C, Chen W.

J Org Chem. 2013 Sep 6;78(17):8531-6. doi: 10.1021/jo401252d. Epub 2013 Aug 27.

PMID:
23944937
7.

Oxidation of alcohols and activated alkanes with Lewis acid-activated TEMPO.

Nguyen TA, Wright AM, Page JS, Wu G, Hayton TW.

Inorg Chem. 2014 Nov 3;53(21):11377-87. doi: 10.1021/ic5018888. Epub 2014 Oct 16.

8.

2-azaadamantane N-oxyl (AZADO) and 1-Me-AZADO: highly efficient organocatalysts for oxidation of alcohols.

Shibuya M, Tomizawa M, Suzuki I, Iwabuchi Y.

J Am Chem Soc. 2006 Jul 5;128(26):8412-3.

PMID:
16802802
9.

Aerobic oxidation of indole carbinols using Fe(NO3)3·9H2O/TEMPO/NaCl as catalysts.

Liu J, Ma S.

Org Biomol Chem. 2013 Jul 7;11(25):4186-93. doi: 10.1039/c3ob40226f.

PMID:
23677005
10.

Efficient and selective aerobic oxidation of alcohols into aldehydes and ketones using ruthenium/TEMPO as the catalytic system.

Dijksman A, Marino-González A, Mairata I Payeras A, Arends IW, Sheldon RA.

J Am Chem Soc. 2001 Jul 18;123(28):6826-33.

PMID:
11448187
11.

Synthesis, characterization and oxidizing properties of a diorgano tellurone carrying bulky aromatic substituents.

Oba M, Okada Y, Nishiyama K, Shimada S, Ando W.

Chem Commun (Camb). 2008 Nov 14;(42):5378-80. doi: 10.1039/b811112j. Epub 2008 Sep 17.

PMID:
18985216
12.

Mechanism of the oxidation of alcohols by oxoammonium cations.

Bailey WF, Bobbitt JM, Wiberg KB.

J Org Chem. 2007 Jun 8;72(12):4504-9. Epub 2007 May 8.

PMID:
17488040
13.

Copper(I)/ABNO-catalyzed aerobic alcohol oxidation: alleviating steric and electronic constraints of Cu/TEMPO catalyst systems.

Steves JE, Stahl SS.

J Am Chem Soc. 2013 Oct 23;135(42):15742-5. doi: 10.1021/ja409241h. Epub 2013 Oct 15.

PMID:
24128057
14.

Direct conversion of alcohols to α-chloro aldehydes and α-chloro ketones.

Jing Y, Daniliuc CG, Studer A.

Org Lett. 2014 Sep 19;16(18):4932-5. doi: 10.1021/ol5024568. Epub 2014 Sep 8.

PMID:
25197943
15.

TEMPO-mediated electrooxidation of primary and secondary alcohols in a microfluidic electrolytic cell.

Hill-Cousins JT, Kuleshova J, Green RA, Birkin PR, Pletcher D, Underwood TJ, Leach SG, Brown RC.

ChemSusChem. 2012 Feb 13;5(2):326-31. doi: 10.1002/cssc.201100601.

PMID:
22337651
16.
17.

Cellulose nanofibrils prepared from softwood cellulose by TEMPO/NaClO/NaClO₂ systems in water at pH 4.8 or 6.8.

Tanaka R, Saito T, Isogai A.

Int J Biol Macromol. 2012 Oct;51(3):228-34. doi: 10.1016/j.ijbiomac.2012.05.016. Epub 2012 May 19.

PMID:
22617623
18.

TEMPO supported on magnetic C/Co-nanoparticles: a highly active and recyclable organocatalyst.

Schätz A, Grass RN, Stark WJ, Reiser O.

Chemistry. 2008;14(27):8262-6. doi: 10.1002/chem.200801001.

PMID:
18666291
19.

Chiral tetranuclear and dinuclear copper(ii) complexes for TEMPO-mediated aerobic oxidation of alcohols: are four metal centres better than two?

Zhang G, Proni G, Zhao S, Constable EC, Housecroft CE, Neuburger M, Zampese JA.

Dalton Trans. 2014 Aug 28;43(32):12313-20. doi: 10.1039/c4dt01224k.

PMID:
24986135
20.

Novel polyaniline-supported molybdenum-catalyzed aerobic oxidation of alcohols to aldehydes and ketones.

Velusamy S, Ahamed M, Punniyamurthy T.

Org Lett. 2004 Dec 23;6(26):4821-4.

PMID:
15606075

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