Literature DB >> 26861673

Advances in Synthetic Applications of Hypervalent Iodine Compounds.

Akira Yoshimura1, Viktor V Zhdankin1.   

Abstract

The preparation, structure, and chemistry of hypervalent iodine compounds are reviewed with emphasis on their synthetic application. Compounds of iodine possess reactivity similar to that of transition metals, but have the advantage of environmental sustainability and efficient utilization of natural resources. These compounds are widely used in organic synthesis as selective oxidants and environmentally friendly reagents. Synthetic uses of hypervalent iodine reagents in halogenation reactions, various oxidations, rearrangements, aminations, C-C bond-forming reactions, and transition metal-catalyzed reactions are summarized and discussed. Recent discovery of hypervalent catalytic systems and recyclable reagents, and the development of new enantioselective reactions using chiral hypervalent iodine compounds represent a particularly important achievement in the field of hypervalent iodine chemistry. One of the goals of this Review is to attract the attention of the scientific community as to the benefits of using hypervalent iodine compounds as an environmentally sustainable alternative to heavy metals.

Entities:  

Year:  2016        PMID: 26861673     DOI: 10.1021/acs.chemrev.5b00547

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  143 in total

1.  Catalytic, Enantioselective 1,2-Difluorination of Cinnamamides.

Authors:  Moriana K Haj; Steven M Banik; Eric N Jacobsen
Journal:  Org Lett       Date:  2019-04-09       Impact factor: 6.005

2.  Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms.

Authors:  Yong-Sok Lee; Joong-Hyun Chun; Milan Hodošček; Victor W Pike
Journal:  Chemistry       Date:  2017-03-02       Impact factor: 5.236

Review 3.  Hypervalent Iodine Reagents in High Valent Transition Metal Chemistry.

Authors:  Felipe Cesar Sousa E Silva; Anthony F Tierno; Sarah E Wengryniuk
Journal:  Molecules       Date:  2017-05-12       Impact factor: 4.411

4.  Enantioselective, Catalytic Fluorolactonization Reactions with a Nucleophilic Fluoride Source.

Authors:  Eric M Woerly; Steven M Banik; Eric N Jacobsen
Journal:  J Am Chem Soc       Date:  2016-10-13       Impact factor: 15.419

5.  Benzimidazopurine nucleosides from N6-aryl adenosine derivatives by PhI(OAc)2-mediated C-N bond formation, no metal needed.

Authors:  Sakilam Satishkumar; Mahesh K Lakshman
Journal:  Chem Commun (Camb)       Date:  2017-02-14       Impact factor: 6.222

6.  Catalytic 1,3-Difunctionalization via Oxidative C-C Bond Activation.

Authors:  Steven M Banik; Katrina M Mennie; Eric N Jacobsen
Journal:  J Am Chem Soc       Date:  2017-06-29       Impact factor: 15.419

7.  Chemoselective Preparation of 1-Iodoalkynes, 1,2-Diiodoalkenes, and 1,1,2-Triiodoalkenes Based on the Oxidative Iodination of Terminal Alkynes.

Authors:  Youzhi Li; Daya Huang; Ju Huang; Yan Liu; Keiji Maruoka
Journal:  J Vis Exp       Date:  2018-09-12       Impact factor: 1.355

8.  I(III)-Catalyzed Oxidative Cyclization-Migration Tandem Reactions of Unactivated Anilines.

Authors:  Tianning Deng; Emily Shi; Elana Thomas; Tom G Driver
Journal:  Org Lett       Date:  2020-10-30       Impact factor: 6.005

9.  Mechanism and Origins of Chemo- and Stereoselectivities of Aryl Iodide-Catalyzed Asymmetric Difluorinations of β-Substituted Styrenes.

Authors:  Biying Zhou; Moriana K Haj; Eric N Jacobsen; K N Houk; Xiao-Song Xue
Journal:  J Am Chem Soc       Date:  2018-11-05       Impact factor: 15.419

10.  (Poly)cationic λ3-Iodane Mediated Oxidative Ring Expansion of Secondary Alcohols.

Authors:  Jennifer C Walters; Anthony F Tierno; Aimee H Dubin; Sarah E Wengryniuk
Journal:  European J Org Chem       Date:  2018-01-31
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