Literature DB >> 21999481

Nucleophilic ortho allylation of aryl and heteroaryl sulfoxides.

Andrew J Eberhart1, Jason E Imbriglio, David J Procter.   

Abstract

Aryl and heteroaryl sulfoxides undergo ortho allylation upon treatment with Tf(2)O and allylsilanes. The method complements the use of sulfoxides to direct ortho-metalation and reaction with electrophiles as it allows allylic carbon nucleophiles to be added ortho to the directing group in a metal-free process. The versatile sulfide adducts can be selectively manipulated using various methods including Kumada-Corriu cross-coupling of the organosulfanyl group.
© 2011 American Chemical Society

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Year:  2011        PMID: 21999481     DOI: 10.1021/ol2025197

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  9 in total

1.  Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts.

Authors:  Daniel Kaiser; Immo Klose; Rik Oost; James Neuhaus; Nuno Maulide
Journal:  Chem Rev       Date:  2019-06-25       Impact factor: 60.622

2.  Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement.

Authors:  Frederico B Souza; Anwar Shamim; Luiz M Z Argomedo; Daniel C Pimenta; Hélio A Stefani
Journal:  Mol Divers       Date:  2015-08-01       Impact factor: 2.943

3.  Sulfoxide-Directed Metal-Free ortho-Propargylation of Aromatics and Heteroaromatics.

Authors:  Andrew J Eberhart; Harry J Shrives; Estela Álvarez; Amandine Carrër; Yuntong Zhang; David J Procter
Journal:  Chemistry       Date:  2015-03-06       Impact factor: 5.236

4.  Nucleophilic ortho-allylation of pyrroles and pyrazoles: an accelerated Pummerer/thio-Claisen rearrangement sequence.

Authors:  Andrew J Eberhart; Claudio Cicoira; David J Procter
Journal:  Org Lett       Date:  2013-07-15       Impact factor: 6.005

5.  Regioselective synthesis of C3 alkylated and arylated benzothiophenes.

Authors:  Harry J Shrives; José A Fernández-Salas; Christin Hedtke; Alexander P Pulis; David J Procter
Journal:  Nat Commun       Date:  2017-03-20       Impact factor: 14.919

6.  Dual vicinal functionalisation of heterocycles via an interrupted Pummerer coupling/[3,3]-sigmatropic rearrangement cascade.

Authors:  Mindaugas Šiaučiulis; Selma Sapmaz; Alexander P Pulis; David J Procter
Journal:  Chem Sci       Date:  2017-11-17       Impact factor: 9.825

7.  Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials.

Authors:  Andrew J Eberhart; Harry Shrives; Yuntong Zhang; Amandine Carrër; Adam V S Parry; Daniel J Tate; Michael L Turner; David J Procter
Journal:  Chem Sci       Date:  2015-11-09       Impact factor: 9.825

8.  Sulfonium-aided coupling of aromatic rings via sigmatropic rearrangement.

Authors:  Hideki Yorimitsu; Gregory J P Perry
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2022       Impact factor: 3.945

9.  Dearomative di- and trifunctionalization of aryl sulfoxides via [5,5]-rearrangement.

Authors:  Mengjie Hu; Yanping Liu; Yuchen Liang; Taotao Dong; Lichun Kong; Ming Bao; Zhi-Xiang Wang; Bo Peng
Journal:  Nat Commun       Date:  2022-08-11       Impact factor: 17.694

  9 in total

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