Literature DB >> 29314580

SuFEx Chemistry of Thionyl Tetrafluoride (SOF4 ) with Organolithium Nucleophiles: Synthesis of Sulfonimidoyl Fluorides, Sulfoximines, Sulfonimidamides, and Sulfonimidates.

Bing Gao1, Suhua Li1, Peng Wu2, John E Moses3, K Barry Sharpless1.   

Abstract

Thionyl tetrafluoride (SOF4 ) is a valuable connective gas for sulfur fluoride exchange (SuFEx) click chemistry that enables multidimensional linkages to be created via sulfur-oxygen and sulfur-nitrogen bonds. Herein, we expand the available SuFEx chemistry of SOF4 to include organolithium nucleophiles, and demonstrate, for the first time, the controlled projection of sulfur-carbon links at the sulfur center of SOF4 -derived iminosulfur oxydifluorides (R1 -N=SOF2 ). This method provides rapid and modular access to sulfonimidoyl fluorides (R1 -N=SOFR2 ), another array of versatile SuFEx connectors with readily tunable reactivity of the S-F handle. Divergent connections derived from these valuable sulfonimidoyl fluoride units are also demonstrated, including the synthesis of sulfoximines, sulfonimidamides, and sulfonimidates.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  SuFEx chemistry; click chemistry; organolithium reagents; sulfonimidoyl fluorides; thionyl tetrafluoride

Mesh:

Substances:

Year:  2018        PMID: 29314580      PMCID: PMC6005182          DOI: 10.1002/anie.201712145

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  32 in total

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2.  A Synthesis of "Dual Warhead" β-Aryl Ethenesulfonyl Fluorides and One-Pot Reaction to β-Sultams.

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3.  Synthesis and functionalization of cyclic sulfonimidamides: a novel chiral heterocyclic carboxylic Acid bioisostere.

Authors:  Nils Pemberton; Henrik Graden; Emma Evertsson; Emma Bratt; Matti Lepistö; Petra Johannesson; Per H Svensson
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4.  Copper-Catalyzed S-C/S-N Bond Interconversions.

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Journal:  Chemistry       Date:  2016-03-04       Impact factor: 5.236

5.  Novel diamide insecticides: sulfoximines, sulfonimidamides and other new sulfonimidoyl derivatives.

Authors:  Christian Gnamm; André Jeanguenat; Ana C Dutton; Christoph Grimm; Daniel P Kloer; Andrew J Crossthwaite
Journal:  Bioorg Med Chem Lett       Date:  2012-04-12       Impact factor: 2.823

6.  Bifluoride-catalysed sulfur(VI) fluoride exchange reaction for the synthesis of polysulfates and polysulfonates.

Authors:  Bing Gao; Linda Zhang; Qinheng Zheng; Feng Zhou; Liana M Klivansky; Jianmei Lu; Yi Liu; Jiajia Dong; Peng Wu; K Barry Sharpless
Journal:  Nat Chem       Date:  2017-06-19       Impact factor: 24.427

7.  Improved method for the iodine(III)-mediated preparation of aryl sulfonimidates.

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8.  SuFEx-based synthesis of polysulfates.

Authors:  Jiajia Dong; Luke Kwisnek; James S Oakdale; K Barry Sharpless; Valery V Fokin
Journal:  Angew Chem Int Ed Engl       Date:  2014-08-05       Impact factor: 15.336

9.  A New, Practical One-Pot Synthesis of Unprotected Sulfonimidamides by Transfer of Electrophilic NH to Sulfinamides.

Authors:  Flavia Izzo; Martina Schäfer; Robert Stockman; Ulrich Lücking
Journal:  Chemistry       Date:  2017-10-09       Impact factor: 5.236

10.  Transfer of Electrophilic NH Using Convenient Sources of Ammonia: Direct Synthesis of NH Sulfoximines from Sulfoxides.

Authors:  Marina Zenzola; Robert Doran; Leonardo Degennaro; Renzo Luisi; James A Bull
Journal:  Angew Chem Int Ed Engl       Date:  2016-04-29       Impact factor: 15.336

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  15 in total

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Authors:  Qinheng Zheng; Jordan L Woehl; Seiya Kitamura; Diogo Santos-Martins; Christopher J Smedley; Gencheng Li; Stefano Forli; John E Moses; Dennis W Wolan; K Barry Sharpless
Journal:  Proc Natl Acad Sci U S A       Date:  2019-09-04       Impact factor: 11.205

2.  Accelerated SuFEx Click Chemistry For Modular Synthesis.

Authors:  Christopher J Smedley; Joshua A Homer; Timothy L Gialelis; Andrew S Barrow; Rebecca A Koelln; John E Moses
Journal:  Angew Chem Int Ed Engl       Date:  2021-12-07       Impact factor: 15.336

3.  SuFExable polymers with helical structures derived from thionyl tetrafluoride.

Authors:  Suhua Li; Gencheng Li; Bing Gao; Sidharam P Pujari; Xiaoyan Chen; Hyunseok Kim; Feng Zhou; Liana M Klivansky; Yi Liu; Hafedh Driss; Dong-Dong Liang; Jianmei Lu; Peng Wu; Han Zuilhof; John Moses; K Barry Sharpless
Journal:  Nat Chem       Date:  2021-08-16       Impact factor: 24.274

4.  Exploiting Configurational Lability in Aza-Sulfur Compounds for the Organocatalytic Enantioselective Synthesis of Sulfonimidamides.

Authors:  Michael J Tilby; Damien F Dewez; Adrian Hall; Carolina Martínez Lamenca; Michael C Willis
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5.  Stereospecific α-(hetero)arylation of sulfoximines and sulfonimidamides.

Authors:  Zachary P Shultz; Thomas Scattolin; Lukasz Wojtas; Justin M Lopchuk
Journal:  Nat Synth       Date:  2022-01-31

6.  A Silyl Sulfinylamine Reagent Enables the Modular Synthesis of Sulfonimidamides via Primary Sulfinamides.

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7.  Additions to N-Sulfinylamines as an Approach for the Metal-free Synthesis of Sulfonimidamides: O-Benzotriazolyl Sulfonimidates as Activated Intermediates.

Authors:  Maximilian Bremerich; Christian M Conrads; Tim Langletz; Carsten Bolm
Journal:  Angew Chem Int Ed Engl       Date:  2019-11-11       Impact factor: 15.336

8.  Identification of simple arylfluorosulfates as potent agents against resistant bacteria.

Authors:  Jiong Zhang; Xiangxiang Zhao; John R Cappiello; Yi Yang; Yunfei Cheng; Guang Liu; Wenjing Fang; Yinzhu Luo; Yu Zhang; Jiajia Dong; Lixin Zhang; K Barry Sharpless
Journal:  Proc Natl Acad Sci U S A       Date:  2021-07-13       Impact factor: 11.205

9.  Silicon-Free SuFEx Reactions of Sulfonimidoyl Fluorides: Scope, Enantioselectivity, and Mechanism.

Authors:  Dong-Dong Liang; Dieuwertje E Streefkerk; Daan Jordaan; Jorden Wagemakers; Jacob Baggerman; Han Zuilhof
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-11       Impact factor: 15.336

10.  Harnessing Sulfinyl Nitrenes: A Unified One-Pot Synthesis of Sulfoximines and Sulfonimidamides.

Authors:  Thomas Q Davies; Michael J Tilby; Jack Ren; Nicholas A Parker; David Skolc; Adrian Hall; Fernanda Duarte; Michael C Willis
Journal:  J Am Chem Soc       Date:  2020-08-25       Impact factor: 15.419

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