2-Iodoxybenzoic acid--a simple oxidant with a dazzling array of potential applications.
Duschek A, Kirsch SF.
Angew Chem Int Ed Engl · journal article · DOI 10.1002/anie.201000873 PUBLICATION REGISTRY
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64 hitsOrganoiodine(V) reagents in organic synthesis.
Zhdankin VV.
J Org Chem · research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/jo1024738Organocatalytic enantioselective β-functionalization of aldehydes by oxidation of enamines and their application in cascade reactions.
Zhang SL, Xie HX, Zhu J, Li H, Zhang XS, Li J, Wang W.
Nat Commun · research support, non-u.s. gov't; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1038/ncomms1214Room-temperature aromatization of tetrahydro-β-carbolines by 2-iodoxybenzoic acid: utility in a total synthesis of eudistomin U.
Panarese JD, Waters SP.
Org Lett · research support, non-u.s. gov't; research-article; journal article; research support, n.i.h., extramural · DOI 10.1021/ol101688xBenziodoxole-based hypervalent iodine reagents for atom-transfer reactions.
Brand JP, Fernández González D, Nicolai S, Waser J.
Chem Commun (Camb) · research support, non-u.s. gov't; review; journal article · DOI 10.1039/c0cc02265aRegiospecific oxidation of polycyclic aromatic phenols to quinones by hypervalent iodine reagents.
Wu A, Duan Y, Xu D, Penning TM, Harvey RG.
Tetrahedron · research-article; journal article · DOI 10.1016/j.tet.2009.12.022New lipophilic piceatannol derivatives exhibiting antioxidant activity prepared by aromatic hydroxylation with 2-iodoxybenzoic acid (IBX).
Bernini R, Barontini M, Spatafora C.
Molecules · research support, non-u.s. gov't; research-article; journal article · DOI 10.3390/molecules14114669Neighboring group stabilization by sigma-holes.
O'Hair RA, Williams CM, Clark T.
J Mol Model · research support, non-u.s. gov't; journal article · DOI 10.1007/s00894-009-0567-1A reactive ortho-quinone generated by tyrosinase-catalyzed oxidation of the skin depigmenting agent monobenzone: self-coupling and thiol-conjugation reactions and possible implications for melanocyte toxicity.
Manini P, Napolitano A, Westerhof W, Riley PA, d'Ischia M.
Chem Res Toxicol · research support, non-u.s. gov't; journal article · DOI 10.1021/tx900018qOxidative conversion of alpha,alpha-disubstituted acetamides to corresponding one-carbon-shorter ketones using hypervalent iodine (lambda5) reagents in combination with tetraethylammonium bromide.
Bellale EV, Bhalerao DS, Akamanchi KG.
J Org Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jo801580gPreparation and X-ray crystal structure of 2-iodyl-N,N-dialkylaniline oxides: first entry into the heterocyclic system of benziodoxazole.
Zhdankin VV, Nemykin VN, Karimov RR, Kazhkenov ZG.
Chem Commun (Camb) · journal article · DOI 10.1039/b813163eEfficient synthesis, liquid chromatography purification, and tandem mass spectrometric characterization of estrogen-modified DNA bases.
Zhang Q, Gross ML.
Chem Res Toxicol · research-article; journal article; research support, n.i.h., extramural · DOI 10.1021/tx800067sOne-pot three-component synthesis of alpha-iminonitriles by IBX/TBAB-mediated oxidative Strecker reaction.
Fontaine P, Chiaroni A, Masson G, Zhu J.
Org Lett · research support, non-u.s. gov't; journal article · DOI 10.1021/ol800199bo-Iodoxybenzoic acid- and tetraethylammonium bromide-mediated oxidative transformation of primary carboxamides to one-carbon dehomologated nitriles.
Bhalerao DS, Mahajan US, Chaudhari KH, Akamanchi KG.
J Org Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jo0619074Alcohols in isonitrile-based multicomponent reaction: Passerini reaction of alcohols in the presence of o-iodoxybenzoic acid.
Ngouansavanh T, Zhu J.
Angew Chem Int Ed Engl · journal article · DOI 10.1002/anie.200600588o-Iodoxybenzoic acid (IBX): pKa and proton-affinity analysis.
Gallen MJ, Goumont R, Clark T, Terrier F, Williams CM.
Angew Chem Int Ed Engl · journal article · DOI 10.1002/anie.200504156A new method for the synthesis of Z-enediones via IBX-mediated oxidative rearrangement of 2-alkynyl alcohol systems.
Crone B, Kirsch SF.
Chem Commun (Camb) · journal article · DOI 10.1039/b515838aIBX-mediated alpha-hydroxylation of alpha-alkynyl carbonyl systems. A convenient method for the synthesis of tertiary alcohols.
Kirsch SF.
J Org Chem · journal article · DOI 10.1021/jo051898jEnhancing 2-iodoxybenzoic acid reactivity by exploiting a hypervalent twist.
Su JT, Goddard WA.
J Am Chem Soc · research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/ja054446xIn situ generation of o-iodoxybenzoic acid (IBX) and the catalytic use of it in oxidation reactions in the presence of Oxone as a co-oxidant.
Thottumkara AP, Bowsher MS, Vinod TK.
Org Lett · journal article · DOI 10.1021/ol050875oSynthesis of the catechols of natural and synthetic estrogens by using 2-iodoxybenzoic acid (IBX) as the oxidizing agent.
Saeed M, Zahid M, Rogan E, Cavalieri E.
Steroids · research support, u.s. gov't, p.h.s.; journal article; research support, n.i.h., extramural · DOI 10.1016/j.steroids.2004.11.005o-Iodoxybenzoic acid (IBX) as a viable reagent in the manipulation of nitrogen- and sulfur-containing substrates: scope, generality, and mechanism of IBX-mediated amine oxidations and dithiane deprotections.
Nicolaou KC, Mathison CJ, Montagnon T.
J Am Chem Soc · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; journal article · DOI 10.1021/ja0400382Mild oxidation of alcohols with O-iodoxybenzoic acid (IBX) in ionic liquid 1-butyl-3-methyl-imidazolium chloride and water.
Liu Z, Chen ZC, Zheng QG.
Org Lett · journal article · DOI 10.1021/ol0351549New reactions of IBX: oxidation of nitrogen- and sulfur-containing substrates to afford useful synthetic intermediates.
Nicolaou KC, Mathison CJ, Montagnon T.
Angew Chem Int Ed Engl · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; journal article · DOI 10.1002/anie.200352076A mild, chemoselective oxidation of sulfides to sulfoxides using o-iodoxybenzoic acid and tetraethylammonium bromide as catalyst.
Shukla VG, Salgaonkar PD, Akamanchi KG.
J Org Chem · journal article · DOI 10.1021/jo034483bMild oxidation of alcohols with o-iodoxybenzoic acid (IBX) in water/acetone mixture in the presence of beta-cyclodextrin.
Surendra K, Krishnaveni NS, Reddy MA, Nageswar YV, Rao KR.
J Org Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jo026751wA simple and advantageous protocol for the oxidation of alcohols with O-iodoxybenzoic acid (IBX).
More JD, Finney NS.
Org Lett · research support, u.s. gov't, p.h.s.; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/ol026427nFacile cleavage of triethylsilyl (TES) ethers using o-iodoxybenzoic acid (IBX) without affecting tert-butyldimethylsilyl (TBS) ethers.
Wu Y, Huang JH, Shen X, Hu Q, Tang CJ, Li L.
Org Lett · research support, non-u.s. gov't; journal article · DOI 10.1021/ol025946nIodine(V) reagents in organic synthesis. Part 3. New routes to heterocyclic compounds via o-iodoxybenzoic acid-mediated cyclizations: generality, scope, and mechanism.
Nicolaou KC, Baran PS, Zhong YL, Barluenga S, Hunt KW, Kranich R, Vega JA.
J Am Chem Soc · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/ja012126hIodine(V) reagents in organic synthesis. Part 4. o-Iodoxybenzoic acid as a chemospecific tool for single electron transfer-based oxidation processes.
Nicolaou KC, Montagnon T, Baran PS, Zhong YL.
J Am Chem Soc · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/ja012127+