Literature DB >> 16788979

Vinyl sulfones: synthetic preparations and medicinal chemistry applications.

D Christopher Meadows1, Jacquelyn Gervay-Hague.   

Abstract

Vinyl sulfones have long been known for their synthetic utility in organic chemistry, easily participating in 1,4-addition reactions and cycloaddition reactions. This functional group has also recently been shown to potently inhibit a variety of enzymatic processes providing unique properties for drug design and medicinal chemistry. This review includes traditional methods used for the synthesis of vinyl sulfones, but focuses mainly on newer reactions applied to vinyl sulfones, including olefin metathesis, conjugate reduction, asymmetric dihydroxylation (AD), and the use of vinyl sulfones to arrive at highly functionalized targets, all illustrating the rich and versatile chemistry this group can efficiently perform. In addition, geminal disulfones are discussed with respect to their formation, reactions, and medicinal applications of this underutilized functional group. 2006 Wiley Periodicals, Inc.

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Year:  2006        PMID: 16788979     DOI: 10.1002/med.20074

Source DB:  PubMed          Journal:  Med Res Rev        ISSN: 0198-6325            Impact factor:   12.944


  20 in total

1.  Anti-inflammatory compounds parthenolide and Bay 11-7082 are direct inhibitors of the inflammasome.

Authors:  Christine Juliana; Teresa Fernandes-Alnemri; Jianghong Wu; Pinaki Datta; Leobaldo Solorzano; Je-Wook Yu; Rong Meng; Andrew A Quong; Eicke Latz; Charles P Scott; Emad S Alnemri
Journal:  J Biol Chem       Date:  2010-01-21       Impact factor: 5.157

2.  Radical-mediated thiodesulfonylation of the vinyl sulfones: Access to (α-fluoro)vinyl sulfides.

Authors:  Pablo R Sacasa; Jessica Zayas; Stanislaw F Wnuk
Journal:  Tetrahedron Lett       Date:  2009-09-23       Impact factor: 2.415

Review 3.  Synthesis and applications of sodium sulfinates (RSO2Na): a powerful building block for the synthesis of organosulfur compounds.

Authors:  Raju Jannapu Reddy; Arram Haritha Kumari
Journal:  RSC Adv       Date:  2021-03-01       Impact factor: 3.361

4.  Azabicyclic vinyl sulfones for residue-specific dual protein labelling.

Authors:  Enrique Gil de Montes; Ester Jiménez-Moreno; Bruno L Oliveira; Claudio D Navo; Pedro M S D Cal; Gonzalo Jiménez-Osés; Inmaculada Robina; Antonio J Moreno-Vargas; Gonçalo J L Bernardes
Journal:  Chem Sci       Date:  2019-03-18       Impact factor: 9.825

5.  Probing of the cis-5-phenyl proline scaffold as a platform for the synthesis of mechanism-based inhibitors of the Staphylococcus aureus sortase SrtA isoform.

Authors:  Konstantin V Kudryavtsev; Matthew L Bentley; Dewey G McCafferty
Journal:  Bioorg Med Chem       Date:  2009-02-13       Impact factor: 3.641

6.  Synthesis of sultam scaffolds via intramolecular oxa-Michael and diastereoselective Baylis-Hillman reactions.

Authors:  Aihua Zhou; Paul R Hanson
Journal:  Org Lett       Date:  2008-06-14       Impact factor: 6.005

7.  Functionalization of immunostimulating complexes (ISCOMs) with lipid vinyl sulfones and their application in immunological techniques and therapy.

Authors:  Teresa Cruz-Bustos; Gloria González-González; Julia Morales-Sanfrutos; Alicia Megía-Fernández; Francisco Santoyo-González; Antonio Osuna
Journal:  Int J Nanomedicine       Date:  2012-12-03

8.  Design and synthesis of polycyclic sulfones via Diels-Alder reaction and ring-rearrangement metathesis as key steps.

Authors:  Sambasivarao Kotha; Rama Gunta
Journal:  Beilstein J Org Chem       Date:  2015-08-06       Impact factor: 2.883

9.  Antimicrobial Effects of Sulfonyl Derivative of 2(5H)-Furanone against Planktonic and Biofilm Associated Methicillin-Resistant and -Susceptible Staphylococcus aureus.

Authors:  Irshad S Sharafutdinov; Elena Y Trizna; Diana R Baidamshina; Maria N Ryzhikova; Regina R Sibgatullina; Alsu M Khabibrakhmanova; Liliya Z Latypova; Almira R Kurbangalieva; Elvira V Rozhina; Mareike Klinger-Strobel; Rawil F Fakhrullin; Mathias W Pletz; Mikhail I Bogachev; Airat R Kayumov; Oliwia Makarewicz
Journal:  Front Microbiol       Date:  2017-11-20       Impact factor: 5.640

10.  Pyrimidine Nucleosides with a Reactive (β-Chlorovinyl)sulfone or (β-Keto)sulfone Group at the C5 Position, Their Reactions with Nucleophiles and Electrophiles, and Their Polymerase-Catalyzed Incorporation into DNA.

Authors:  Sazzad H Suzol; A Hasan Howlader; Zhiwei Wen; Yaou Ren; Eduardo E Laverde; Carol Garcia; Yuan Liu; Stanislaw F Wnuk
Journal:  ACS Omega       Date:  2018-04-16
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