Kyselina jodoxybenzoová (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kyselina jodoxybenzoová" in Czech language version.

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13doi.org

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1caltech.edu

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authors.library.caltech.edu

J. T. Su; W. A. Goddard. Enhancing 2-Iodoxybenzoic Acid Reactivity by Exploiting a Hypervalent Twist. Journal of the American Chemical Society. 2005, s. 1414–14147. Dostupné online. DOI 10.1021/ja054446x. PMID 16218584.

doi.org

dx.doi.org

M. Frigerio; M. Santagostino; S. Sputore. A User-Friendly Entry to 2-Iodoxybenzoic Acid (IBX). Journal of Organic Chemistry. 1999, s. 4537–4538. DOI 10.1021/jo9824596.
D. B. Dess; J. C. Martin. A Useful 12-I-5 Triacetoxyperiodinane (the Dess–Martin Periodinane) for the Selective Oxidation of Primary or Secondary Alcohols and a Variety of Related 12-I-5 Species. Journal of the American Chemical Society. 1991, s. 7277–7287. DOI 10.1021/ja00019a027.
J. T. Su; W. A. Goddard. Enhancing 2-Iodoxybenzoic Acid Reactivity by Exploiting a Hypervalent Twist. Journal of the American Chemical Society. 2005, s. 1414–14147. Dostupné online. DOI 10.1021/ja054446x. PMID 16218584.
M. J. Gallen; R. Goumont; T. Clark; F. Terrier; C. M. Williams. o-Iodoxybenzoic Acid (IBX): pK_a and Proton-Affinity Analysis. Angewandte Chemie International Edition. 2006, s. 2929–2934. DOI 10.1002/anie.200504156. PMID 16566050.
D. K. Mohapatra; G. S. Yellol. Asymmetric Total Synthesis of Eicosanoid. Arkivoc. 2005, s. 144–155. DOI 10.3998/ark.5550190.0006.316.
J. D. More; N. S. Finney. A Simple and Advantageous Protocol for the Oxidation of Alcohols with o-Iodoxybenzoic Acid (IBX). Organic Letters. 2002, s. 3001–3003. DOI 10.1021/ol026427n. PMID 12182609.
S. Van Arman. 2-Methyl-2-propanol as solvent for o-iodoxybenzoic acid (IBX) oxidation of 1˚ alcohols to aldehydes. Tetrahedron Letters. 2009, s. 4693–4695. DOI 10.1016/j.tetlet.2009.06.045.
K. C. Nicolaou; T. Montagnon; P. S. Baran; Y.-L. Zhong. Iodine(V) Reagents in Organic Synthesis. Part 4. o-Iodoxybenzoic Acid as a Chemospecific Tool for Single Electron Transfer-Based Oxidation Processes. Journal of the American Chemical Society. 2002-03-01, s. 2245–2258. ISSN 0002-7863. DOI 10.1021/ja012127+. PMID 11878978.
M. Frigerio; M. Santagostino. A Mild Oxidizing Reagent for Alcohols and 1,2-Diols: o-Iodoxybenzoic Acid (IBX) in DMSO. Tetrahedron Letters. 1994, s. 8019–8022. DOI 10.1016/0040-4039(94)80038-3.
J. N. Moorthy; N. Singhal; K. Senapati. Oxidative Cleavage of Vicinal Diols: IBX can do what Dess–Martin Periodinane (DMP) can. Organic & Biomolecular Chemistry. 2007, s. 767–771. DOI 10.1039/b618135j. PMID 17315062.
S. F. Kirsch. IBX-Mediated α-Hydroxylation of α-Alkynyl Carbonyl Systems. A Convenient Method for the Synthesis of Tertiary Alcohols. Journal of Organic Chemistry. 2005, s. 10210-10212. DOI 10.1021/jo051898j. PMID 16292876.
S. F. Kirsch; A. Duschek. Novel Oxygenations with IBX. Chemistry: A European Journal. 2009, s. 10713-10717. DOI 10.1002/chem.200901867. PMID 19760735.
S. L. Bartlett; C. M. Beaudry. High Yielding Oxidation of β-Hydroxyketones to β-Diketones Using o-Iodoxybenzoic Acid.Chybí název periodika! 2011, s. 9852–9855. DOI 10.1021/jo201810c. PMID 22023037.

nih.gov

ncbi.nlm.nih.gov

J. T. Su; W. A. Goddard. Enhancing 2-Iodoxybenzoic Acid Reactivity by Exploiting a Hypervalent Twist. Journal of the American Chemical Society. 2005, s. 1414–14147. Dostupné online. DOI 10.1021/ja054446x. PMID 16218584.
M. J. Gallen; R. Goumont; T. Clark; F. Terrier; C. M. Williams. o-Iodoxybenzoic Acid (IBX): pK_a and Proton-Affinity Analysis. Angewandte Chemie International Edition. 2006, s. 2929–2934. DOI 10.1002/anie.200504156. PMID 16566050.
J. D. More; N. S. Finney. A Simple and Advantageous Protocol for the Oxidation of Alcohols with o-Iodoxybenzoic Acid (IBX). Organic Letters. 2002, s. 3001–3003. DOI 10.1021/ol026427n. PMID 12182609.
K. C. Nicolaou; T. Montagnon; P. S. Baran; Y.-L. Zhong. Iodine(V) Reagents in Organic Synthesis. Part 4. o-Iodoxybenzoic Acid as a Chemospecific Tool for Single Electron Transfer-Based Oxidation Processes. Journal of the American Chemical Society. 2002-03-01, s. 2245–2258. ISSN 0002-7863. DOI 10.1021/ja012127+. PMID 11878978.
J. N. Moorthy; N. Singhal; K. Senapati. Oxidative Cleavage of Vicinal Diols: IBX can do what Dess–Martin Periodinane (DMP) can. Organic & Biomolecular Chemistry. 2007, s. 767–771. DOI 10.1039/b618135j. PMID 17315062.
S. F. Kirsch. IBX-Mediated α-Hydroxylation of α-Alkynyl Carbonyl Systems. A Convenient Method for the Synthesis of Tertiary Alcohols. Journal of Organic Chemistry. 2005, s. 10210-10212. DOI 10.1021/jo051898j. PMID 16292876.
S. F. Kirsch; A. Duschek. Novel Oxygenations with IBX. Chemistry: A European Journal. 2009, s. 10713-10717. DOI 10.1002/chem.200901867. PMID 19760735.
S. L. Bartlett; C. M. Beaudry. High Yielding Oxidation of β-Hydroxyketones to β-Diketones Using o-Iodoxybenzoic Acid.Chybí název periodika! 2011, s. 9852–9855. DOI 10.1021/jo201810c. PMID 22023037.

pubchem.ncbi.nlm.nih.gov

https://pubchem.ncbi.nlm.nih.gov/compound/339496

orgsyn.org

BOECKMAN, R. K.; SHAO, P.; MULLINS, J. J. Dess–Martin periodinane: 1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one. Org. Synth.. 2000, s. 141. Dostupné online. ; Coll. Vol.. S. 696.

worldcat.org

K. C. Nicolaou; T. Montagnon; P. S. Baran; Y.-L. Zhong. Iodine(V) Reagents in Organic Synthesis. Part 4. o-Iodoxybenzoic Acid as a Chemospecific Tool for Single Electron Transfer-Based Oxidation Processes. Journal of the American Chemical Society. 2002-03-01, s. 2245–2258. ISSN 0002-7863. DOI 10.1021/ja012127+. PMID 11878978.