Literature DB >> 31185136

Sulfones as Chemical Chameleons: Versatile Synthetic Equivalents of Small-Molecule Synthons.

Barry M Trost1, Christopher A Kalnmals1.   

Abstract

Sulfones are flexible functional groups that can act as nucleophiles, electrophiles, or even radicals. Changing the reaction conditions can completely alter the reactivity of a sulfonyl group, and as a result, molecules bearing multiple sulfones are versatile building blocks. This Review highlights the unique ability of 1,1- and 1,2-bis(sulfones) to masquerade as a vast array of reactive synthons including methane polyanions, vinyl cations, and all-carbon dipoles that would be difficult or impossible to access directly.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  C1 building blocks; reactive intermediates; sulfur; synthetic methods; umpolung

Year:  2019        PMID: 31185136     DOI: 10.1002/chem.201902019

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  10 in total

1.  Thianthrenium-Enabled Sulfonylation via Electron Donor-Acceptor Complex Photoactivation.

Authors:  Albert Granados; María Jesús Cabrera-Afonso; Marcos Escolano; Shorouk O Badir; Gary A Molander
Journal:  Chem Catal       Date:  2022-04-05

2.  Titanium Radical Redox Catalysis: Recent Innovations in Catalysts, Reactions, and Modes of Activation.

Authors:  Xiangyu Wu; Yejin Chang; Song Lin
Journal:  Chem       Date:  2022-07-01       Impact factor: 25.832

3.  Phenyl Sulfones: A Route to a Diverse Family of Trisubstituted Cyclohexenes from Three Independent Nucleophilic Additions.

Authors:  Spenser R Simpson; Paolo Siano; Daniel J Siela; Louis A Diment; Brian C Song; Karl S Westendorff; Megan N Ericson; Kevin D Welch; Diane A Dickie; W Dean Harman
Journal:  J Am Chem Soc       Date:  2022-05-20       Impact factor: 16.383

Review 4.  Recent Progress and Emerging Technologies towards a Sustainable Synthesis of Sulfones.

Authors:  Shuai Liang; Kamil Hofman; Marius Friedrich; Julian Keller; Georg Manolikakes
Journal:  ChemSusChem       Date:  2021-10-13       Impact factor: 9.140

5.  An efficient approach for the synthesis of novel methyl sulfones in acetic acid medium and evaluation of antimicrobial activity.

Authors:  Gollapudi Ravi Kumar; Chandra Rao Dasireddy; Ravi Varala; Vijay Kotra; Hari Babu Bollikolla
Journal:  Turk J Chem       Date:  2020-10-26       Impact factor: 1.239

6.  A Titanium-Catalyzed Reductive α-Desulfonylation.

Authors:  Christoph Kern; Jan Selau; Jan Streuff
Journal:  Chemistry       Date:  2021-03-05       Impact factor: 5.236

7.  Three-component three-bond forming cascade via palladium photoredox catalysis.

Authors:  Peter Bellotti; Maximilian Koy; Christian Gutheil; Steffen Heuvel; Frank Glorius
Journal:  Chem Sci       Date:  2020-12-07       Impact factor: 9.825

8.  Divergent reactivity of sulfinates with pyridinium salts based on one- versus two-electron pathways.

Authors:  Myojeong Kim; Euna You; Seongjin Park; Sungwoo Hong
Journal:  Chem Sci       Date:  2021-03-31       Impact factor: 9.825

9.  Isolation and structure determination of a tetrameric sulfonyl dilithio methandiide in solution based on crystal structure analysis and 6Li/13C NMR spectroscopic data.

Authors:  Jürgen Vollhardt; Hans Jörg Lindner; Hans-Joachim Gais
Journal:  Beilstein J Org Chem       Date:  2020-08-21       Impact factor: 2.883

10.  Silyloxymethanesulfinate as a sulfoxylate equivalent for the modular synthesis of sulfones and sulfonyl derivatives.

Authors:  Dae-Kwon Kim; Hyun-Suk Um; Hoyoon Park; Seonwoo Kim; Jin Choi; Chulbom Lee
Journal:  Chem Sci       Date:  2020-10-22       Impact factor: 9.825

  10 in total

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