Relevant bibliographies by topics / Novel hypervalent iodine

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Novel hypervalent iodine'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Novel hypervalent iodine"

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Zhang, Chi, Xiao-Guang Yang, Ze-Nan Hu, Meng-Cheng Jia, and Feng-Huan Du. "Recent Advances and the Prospect of Hypervalent Iodine Chemistry." Synlett 32, no. 13 (2021): 1289–96. http://dx.doi.org/10.1055/a-1492-4943.

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AbstractNowadays, hypervalent iodine chemistry has remarkably advanced in parallel with the emergence of novel hypervalent iodine reagents. Hypervalent iodine reagents, due to their outstanding characteristics including rich reactivities, excellent chemoselectivity, stability, and environmental friendliness, are becoming more and more popular in the synthetic organic chemistry. In this Account, a number of recent elegant research works and our perspective on the future of hypervalent iodine chemistry is presented.1 Introduction2 Recent Advances and Discussion2.1 Novel Reactivities of Hypervale
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Moriarty, Robert M., Raju Penmasta, and Indra Prakash. "Novel pentafluorophenyl hypervalent iodine reagents." Tetrahedron Letters 28, no. 8 (1987): 877–80. http://dx.doi.org/10.1016/s0040-4039(01)81012-1.

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Xing, Linlin, Yong Zhang, and Yunfei Du. "Hypervalent Iodine-Mediated Synthesis of Spiroheterocycles via Oxidative Cyclization." Current Organic Chemistry 23, no. 1 (2019): 14–37. http://dx.doi.org/10.2174/1385272822666181211122802.

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Hypervalent iodine reagents have been widely used in the construction of many important building blocks and privileged scaffolds of bioactive natural products. This review article aims to briefly discuss strategies that have used hypervalent iodine reagents as oxidants to synthesize spiroheterocyclic compounds and to stimulate further study for novel syntheses of spiroheterocyclic core structures using hypervalent iodine reagents under metal-free conditions.
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Farnham, William B., and Joseph C. Calabrese. "Novel hypervalent (10-I-2) iodine structures." Journal of the American Chemical Society 108, no. 9 (1986): 2449–51. http://dx.doi.org/10.1021/ja00269a055.

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Zhang, Guangtao, Yuanxun Wang, Jun Xu, et al. "A new hypervalent iodine(iii/v) oxidant and its application to the synthesis of 2H-azirines." Chemical Science 11, no. 4 (2020): 947–53. http://dx.doi.org/10.1039/c9sc05536c.

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The reaction of o-nitroiodobenzene and mCPBA in AcOH was found to afford a novel hypervalent iodine compound which both iodine(iii) and iodine(v) moieties coexist. This new reagent is proved to be effective in realizing the synthesis of 2H-azirines.
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Zhang, Yang, Hua Tan та Weibing Liu. "Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids". RSC Advances 7, № 85 (2017): 54017–20. http://dx.doi.org/10.1039/c7ra11875a.

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Wang, Ruijia, Yuejun OuYang, Chonghui Xu, et al. "Hypervalent iodine-triggered transformation of homopropargyl sulfonamides into dihalo-2,3-dihydropyrroles." Organic & Biomolecular Chemistry 15, no. 4 (2017): 796–800. http://dx.doi.org/10.1039/c6ob02536f.

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Mizar, Pushpak, Aragorn Laverny, Mohammad El-Sherbini, et al. "Enantioselective Diamination with Novel Chiral Hypervalent Iodine Catalysts." Chemistry - A European Journal 20, no. 32 (2014): 9910–13. http://dx.doi.org/10.1002/chem.201403891.

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Evans, P. Andrew, and Thomas A. Brandt. "Novel haloacetoxylation of 1,4-dimethoxynaphthalenes using hypervalent iodine chemistry." Tetrahedron Letters 37, no. 36 (1996): 6443–46. http://dx.doi.org/10.1016/0040-4039(96)01427-x.

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Gupta, Preeti, and Amiya Prasad Bhaduri. "Novel Oxidation of Proline Derivatives to Pyrroles by Hypervalent Iodine." Synthetic Communications 28, no. 17 (1998): 3151–57. http://dx.doi.org/10.1080/00397919808004414.

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Dissertations / Theses on the topic "Novel hypervalent iodine"

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Khan, Zulfiqar Ali. "Novel iodine mediated carbocyclisations and hypervalent iodine(III) reagents." Thesis, Cardiff University, 2010. http://orca.cf.ac.uk/54137/.

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The first chapter focuses on the introduction of iodine mediated carbocyclisations and their applications continue to present a stimulating challenge in target- and diversity-oriented synthesis. The second chapter discusses applications and brief literature overview about classical approaches towards the syntheses of indene derivatives. Herein the syntheses of 3-iodo-1 H-indene derivatives via iodonium-promoted 5-endo-dig carbocyclisation of 2-substituted ethynylmalonates as a key starting material are described. Within this study, we were able to show that the 3-iodo-1 H-indene can be used as
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Edmunds, J. J. "Novel fluorination reactions via hypervalent iodine reagents." Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/47045.

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Cooke, Michael Liam. "Development of novel arylation and alkenylation reactions using hypervalent iodine reagents and copper catalysis." Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609862.

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Ilchenko, Nadia O. "Novel Applications of Benziodoxole Reagents in the Synthesis of Organofluorine Compounds." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-136207.

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This thesis concerns method development of new synthetic routes by applying electrophilic hypervalent iodine reagents, such as trifluoromethyl-benziodoxole (Togni reagent) and fluoro-benziodoxole. The first project involved the addition of an oxygen moiety and trifluoromethyl group across double and triple bonds (both groups derived from the hypervalent iodine reagent). We observed that electron donating substituents on the aromatic ring of the substrate accelerated the oxytrifluoromethylation reaction. This transformation was further expanded to halo-trifluoromethylation reaction of a vinyl s
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Phipps, Robert James. "Copper catalysis as a tool for developing novel and selective arylation reactions using hypervalent iodine reagents." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608863.

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Chun, Joong-Hyun. "NMR Studies of the Hydration Equilibria of Mesylate and Dialkyl Phosphate Derivatives of Acetone; and Investigations of Novel Hypervalent Iodine Compounds." University of Akron / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=akron1131685679.

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Potturi, Hima. "SYNTHESES AND ESTROGENICITY STUDY OF DIETHYLSTILBESTROL AND BISPHENOL-A ANALOGS AS POTENTIAL REPLACEMENT FOR BISPHENOL-A AND INVESTIGATION ON NOVEL REACTIONS INDUCED BY IODANE/QUATERNARY AMMONIUM HALIDES." OpenSIUC, 2011. https://opensiuc.lib.siu.edu/dissertations/403.

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Dynamic isomerization of diethylstilbestrol (DES) makes it difficult to ascertain the active estrogen between its E and Z isomers. An indirect approach has been used in this project to identify the active estrogen. Methoxylated E- and Z-DES (13 and 14) and 9,10-diethylphenanthrene-3,6-diol (15), a closed ring analog of Z-DES, were synthesized and tested for their estrogenicity. The estrogenicity of 13 is higher than that of 14 and 15, which indicates that E-DES is more estrogenic than Z-DES. Dimethylstilbestrol (16), another analog of DES, was also synthesized and tested. Its estrogenicity is
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Ahmad, Anees. "Exploring the iodine(III)-mediated ring contraction: new substrates, novel conditions and asymmetric reactions." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-29092015-145020/.

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In the first section this thesis includes the reactivity of various oxygen-containing benzofused cyclic alkenes with HTIB (Hydroxy(tosyloxy)iodobenzene). Instead of getting ring contraction products, 2H-chromene resulted in 4H-chromenes together with trans-addition products. Only cis-addition products were isolated from 4-methyl-2H-chromene. Ring contraction was observed in dihydrobenzoxepines and 2,2-dimethyl-2H-chromenes giving functionalized chromanes and benzofurans, respectively. In the second part, the ring contraction of 1,2-dihydronaphthalenes using HTIB was expanded to substrates be
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Fumbatha, Sinethemba. "Development of novel hypervalent iodine conjugation strategies towards pneumococcal conjugate vaccines." 2013. http://hdl.handle.net/11394/3551.

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Masters of Science<br>Invasive pneumococcal disease (IPD), which includes potentially fatal conditions such as meningitis, septicaemia and pneumonia poses a threat in children aged <5 years, pneumonia being the leading cause of child mortality worldwide. Even though capsular polysaccharides are the main antigens involved in the immunity to encapsulated bacteria, it was found that in children in that age group, the immune system was unresponsive. Conjugate vaccines however induce immunologic memory and provide long-term protective immunity. Therefore the aim of this project was to develop nove
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Macara, João Cristóvão Santos Silva. "Investigation of novel sulfonylation methods." Master's thesis, 2017. http://hdl.handle.net/10362/25418.

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