Home / Publications / Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds

Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds

65
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Yusubov M. S. O., Zhdankin V. V. Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds // Mendeleev Communications. 2010. Vol. 20. No. 4. pp. 185-191.
GOST all authors (up to 50) Copy
Yusubov M. S. O., Zhdankin V. V. Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds // Mendeleev Communications. 2010. Vol. 20. No. 4. pp. 185-191.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2010.06.001
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.06.001
TI - Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds
T2 - Mendeleev Communications
AU - Yusubov, Mehman Suleiman ogly
AU - Zhdankin, Viktor Vladimirovich
PY - 2010
DA - 2010/06/16
PB - Mendeleev Communications
SP - 185-191
IS - 4
VL - 20
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2010_Yusubov,
author = {Mehman Suleiman ogly Yusubov and Viktor Vladimirovich Zhdankin},
title = {Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds},
journal = {Mendeleev Communications},
year = {2010},
volume = {20},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.06.001},
number = {4},
pages = {185--191},
doi = {10.1016/j.mencom.2010.06.001}
}
MLA
Cite this
MLA Copy
Yusubov, Mehman Suleiman ogly, and Viktor Vladimirovich Zhdankin. “Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds.” Mendeleev Communications, vol. 20, no. 4, Jun. 2010, pp. 185-191. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.06.001.
Views / Downloads
1 / 7

Abstract

Recent advances in the development of polymer-supported iodine(V) oxidants, recyclable monomeric hypervalent iodine(III) reagents and catalytic systems based on hypervalent iodine compounds are discussed. These efficient and environmentally friendly reagents and catalysts are particularly useful for oxidative transformations of alcohols to carbonyl compounds and for oxidations at the benzylic position.

References

1.
Hypervalent Iodine Chemistry, ed. T. Wirth, Springer-Verlag, Berlin, 2003.
2.
Chemistry of polyvalent iodine.
Zhdankin V.V., Stang P.J.
Chemical Reviews, 2008
6.
U. Ladziata and V. V. Zhdankin, Synlett, 2007, 527.
7.
Hypervalent Iodine Goes Catalytic
Richardson R.D., Wirth T.
Angewandte Chemie - International Edition, 2006
8.
Hypervalent iodine-mediated oxidation of alcohols.
Uyanik M., Ishihara K.
Chemical Communications, 2009
14.
Preparation of Dess–Martin periodinane—the role of the morphology of 1-hydroxy-1,2-benziodoxol-3(1H )-one 1-oxide precursor
Stevenson P.J., Treacy A.B., Nieuwenhuyzen M.
Journal of the Chemical Society Perkin Transactions 2, 1997
16.
IBX Amides: A New Family of Hypervalent Iodine Reagents
Zhdankin V.V., Koposov A.Y., Netzel B.C., Yashin N.V., Rempel B.P., Ferguson M.J., Tykwinski R.R.
Angewandte Chemie - International Edition, 2003
18.
Esters of 2-Iodoxybenzoic Acid:  Hypervalent Iodine Oxidizing Reagents with a Pseudobenziodoxole Structure
Zhdankin V.V., Koposov A.Y., Litvinov D.N., Ferguson M.J., McDonald R., Luu T., Tykwinski R.R.
Journal of Organic Chemistry, 2005
19.
Synthesis, Structure, and Chemoselective Reactivity ofN-(2-Iodylphenyl)acylamides: Hypervalent Iodine Reagents Bearing a Pseudo-Six-Membered Ring Scaffold
Ladziata U., Koposov A.Y., Lo K.Y., Willging J., Nemykin V.N., Zhdankin V.V.
Angewandte Chemie - International Edition, 2005
20.
2-Iodylphenol Ethers:  Preparation, X-ray Crystal Structure, and Reactivity of New Hypervalent Iodine(V) Oxidizing Reagents
Koposov A.Y., Karimov R.R., Geraskin I.M., Nemykin V.N., Zhdankin V.V.
Journal of Organic Chemistry, 2006
21.
2-Iodoxybenzenesulfamides: new pseudobenziodoxole-based hypervalent iodine reagents
22.
Zhdankin V.V., Goncharenko R.N., Litvinov D.N., Koposov A.Y.
Arkivoc, 2004
24.
10.1016/j.mencom.2010.06.001_bib24
Koposov
Synthesis, 2005
25.
Green Chemistry Education: Changing the Course of Chemistry, eds. P. T. Anastas, I. J. Levy and K. E. Parent, ACS Symposium Series, 2009.
26.
Recoverable Catalysts and Reagents Using Recyclable Polystyrene-Based Supports
McNamara C.A., Dixon M.J., Bradley M.
Chemical Reviews, 2002
30.
10.1016/j.mencom.2010.06.001_bib30
Kim
Synlett, 2005
34.
Polymer supported perruthenate (PSP): a new oxidant for clean organic synthesis
Hinzen B., Ley S.V.
Journal of the Chemical Society Perkin Transactions 1, 1997
35.
Preparation and Reactivity of Polymer-Supported 2-Iodylphenol Ethers, an Efficient Recyclable Oxidizing System
Karimov R.R., Kazhkenov Z.M., Modjewski M.J., Peterson E.M., Zhdankin V.V.
Journal of Organic Chemistry, 2007
36.
Preparation and Reactivity of 1,3,5,7-Tetrakis[4-(diacetoxyiodo)phenyl]adamantane, a Recyclable Hypervalent Iodine(III) Reagent
Tohma H., Maruyama A., Maeda A., Maegawa T., Dohi T., Shiro M., Morita T., Kita Y.
Angewandte Chemie - International Edition, 2004
39.
10.1016/j.mencom.2010.06.001_bib39
Yusubov
Synlett, 2007
41.
Preparation and X-ray Structures of 3-[Bis(trifluoroacetoxy)iodo]benzoic Acid and 3-[Hydroxy(tosyloxy)iodo]benzoic Acid:  New Recyclable Hypervalent Iodine Reagents
42.
Reactivity and Synthetic Utility of 1-(Arenesulfonyloxy)benziodoxolones
Muraki T., Togo H., Yokoyama M.
Journal of Organic Chemistry, 1999
43.
Iodobenzene-catalyzed alpha-acetoxylation of ketones. in situ generation of hypervalent (diacyloxyiodo)benzenes using m-chloroperbenzoic acid.
Ochiai M., Takeuchi Y., Katayama T., Sueda T., Miyamoto K.
Journal of the American Chemical Society, 2005
44.
10.1016/j.mencom.2010.06.001_bib44
Sheng
Synthesis, 2007
46.
10.1016/j.mencom.2010.06.001_bib46
Richardson
Synlett, 2007
49.
Versatile Hypervalent-Iodine(III)-Catalyzed Oxidations withm-Chloroperbenzoic Acid as a Cooxidant
Dohi T., Maruyama A., Yoshimura M., Morimoto K., Tohma H., Kita Y.
Angewandte Chemie - International Edition, 2005
51.
A New H2O2/Acid Anhydride System for the Iodoarene-Catalyzed C−C Bond-Forming Reactions of Phenols
Dohi T., Minamitsuji Y., Maruyama A., Hirose S., Kita Y.
Organic Letters, 2008
52.
10.1016/j.mencom.2010.06.001_bib52
Moroda
Synthesis, 2008
54.
Asymmetric Hydroxylative Phenol Dearomatization through In Situ Generation of Iodanes from Chiral Iodoarenes andm-CPBA
Quideau S., Lyvinec G., Marguerit M., Bathany K., Ozanne-Beaudenon A., Buffeteau T., Cavagnat D., Chénedé A.
Angewandte Chemie - International Edition, 2009
55.
A Chiral Hypervalent Iodine(III) Reagent for Enantioselective Dearomatization of Phenols
Dohi T., Maruyama A., Takenaga N., Senami K., Minamitsuji Y., Fujioka H., Caemmerer S., Kita Y.
Angewandte Chemie - International Edition, 2008
57.
The Discovery of Catalytic Enantioselective Polyvalent Iodine Mediated Reactions
Ngatimin M., Lupton D.W.
Australian Journal of Chemistry, 2010
60.
10.1016/j.mencom.2010.06.001_bib60
Schulze
Synthesis, 2006
62.
10.1016/j.mencom.2010.06.001_bib62
Ojha
Synlett, 2009
63.
Preparation and Reductive Decomposition of 2-Iodoxybenzenesulfonic Acid. X-ray Crystal Structure of 1-Hydroxy-1H-1,2,3-benziodoxathiole 3,3-Dioxide
Koposov A.Y., Litvinov D.N., Zhdankin V.V., Ferguson M.J., McDonald R., Tykwinski R.R.
European Journal of Organic Chemistry, 2006
65.
RuCl3-Catalyzed Oxidation of Iodoarenes with Peracetic Acid:  New Facile Preparation of Iodylarenes
Koposov A.Y., Karimov R.R., Pronin A.A., Skrupskaya T., Yusubov M.S., Zhdankin V.V.
Journal of Organic Chemistry, 2006
71.
Organic iodine(V) compounds as terminal oxidants in iron(III) phthalocyanine catalyzed oxidation of alcohols
Geraskin I.M., Luedtke M.W., Neu H.M., Nemykin V.N., Zhdankin V.V.
Tetrahedron Letters, 2008
75.
1-Amido-3-(1H)-1,2-benziodoxoles: Stable amidoiodanes and reagents for direct amidation of organic substrates
Zhdankin V.V., McSherry M., Mismash B., Bolz J.T., Woodward J.K., Arbit R.M., Erickson S.
Tetrahedron Letters, 1997
77.
1-[Hydroxy(sulfonyloxy)iodo]-1H,1H-perfluoroalkanes:  Stable, Fluoroalkyl Analogs of Koser's Reagent
78.
1-Cyano-3-(1H)-1,2-benziodoxols: stable cyanoiodinanes and efficient reagents for direct N-alkyl cyanation of N,N-dialkylarylamines
Zhdankin V.V., Kuehl C.J., Krasutsky A.P., Bolz J.T., Mismash B., Woodward J.K., Simonsen A.J.
Tetrahedron Letters, 1995
79.
Direct Azidation of Adamantane and Norbornane by Stable Azidoiodinanes
80.
Preparation, X-ray Crystal Structure, and Chemistry of Stable AzidoiodinanesDerivatives of Benziodoxole
Zhdankin V.V., Krasutsky A.P., Kuehl C.J., Simonsen A.J., Woodward J.K., Mismash B., Bolz J.T.
Journal of the American Chemical Society, 1996
81.
Structure and Chemistry of Acetoxybenziodazole. Acid-Catalyzed Rearrangement of Benziodazoles to 3-Iminobenziodoxoles
Zhdankin V.V., Arbit R.M., McSherry M., Mismash B., Young V.G.
Journal of the American Chemical Society, 1997
83.
Secondary Bonding-Directed Self-Assembly of Amino Acid Derived Benziodazoles:  Synthesis and Structure of Novel Hypervalent Iodine Macrocycles
Zhdankin V.V., Koposov A.E., Smart J.T., Tykwinski R.R., McDonald R., Morales-Izquierdo A.
Journal of the American Chemical Society, 2001
84.
Synthesis and Structure of Amino Acid-Derived Benziodazoles:  New Hypervalent Iodine Heterocycles
Zhdankin V.V., Koposov A.Y., Su L., Boyarskikh V.V., Netzel B.C., Young V.G.
Organic Letters, 2003
85.
Preparation, Structure, and Unexpected Chemistry of Phosphoranyl-Derived Benziodoxoles
Zhdankin V.V., Maydanovych O., Herschbach J., McDonald R., Tykwinski R.R.
Journal of the American Chemical Society, 2002
86.
Preparation and Chemistry of Phosphoranyl-Derived Iodanes
Zhdankin V.V., Maydanovych O., Herschbach J., Bruno J., Matveeva E.D., Zefirov N.S.
Journal of Organic Chemistry, 2003
88.
Preparation and Structure of Oligomeric Iodosylbenzene Sulfate (PhIO)3·SO3: Stable and Water-Soluble Analog of Iodosylbenzene
Koposov A.Y., Netzel B.C., Yusubov M.S., Nemykin V.N., Nazarenko A.Y., Zhdankin V.V.
European Journal of Organic Chemistry, 2007