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Beyond the Pummerer reaction: recent developments in Thionium ion chemistry

Research output: Contribution to Journal/Magazine › Literature review › peer-review

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Beyond the Pummerer reaction: recent developments in Thionium ion chemistry. / Smith, Laura H. S.; Coote, Susannah C.; Sneddon, Helen F. et al.
In: Angewandte Chemie International Edition, Vol. 49, No. 34, 09.08.2010, p. 5832-5844.

Research output: Contribution to Journal/Magazine › Literature review › peer-review

Harvard

Smith, LHS, Coote, SC, Sneddon, HF & Procter, DJ 2010, 'Beyond the Pummerer reaction: recent developments in Thionium ion chemistry', Angewandte Chemie International Edition, vol. 49, no. 34, pp. 5832-5844. https://doi.org/10.1002/anie.201000517

APA

Smith, L. H. S., Coote, S. C., Sneddon, H. F., & Procter, D. J. (2010). Beyond the Pummerer reaction: recent developments in Thionium ion chemistry. Angewandte Chemie International Edition, 49(34), 5832-5844. https://doi.org/10.1002/anie.201000517

Vancouver

Smith LHS, Coote SC, Sneddon HF, Procter DJ. Beyond the Pummerer reaction: recent developments in Thionium ion chemistry. Angewandte Chemie International Edition. 2010 Aug 9;49(34):5832-5844. doi: 10.1002/anie.201000517

Author

Smith, Laura H. S. ; Coote, Susannah C. ; Sneddon, Helen F. et al. / Beyond the Pummerer reaction : recent developments in Thionium ion chemistry. In: Angewandte Chemie International Edition. 2010 ; Vol. 49, No. 34. pp. 5832-5844.

Bibtex

@article{36f919b5da1e4ef392dad064874bf58c,
title = "Beyond the Pummerer reaction: recent developments in Thionium ion chemistry",
abstract = "Since the early 1960s the Pummerer reaction has evolved to become an indispensable tool for synthesis, and continues to serve as a source of inspiration for organic chemists. In recent years, many exciting advances have demonstrated the broad scope and synthetic utility of Pummerer methodology and the versatility of thionium ion intermediates.",
keywords = "cyclization, heterocycles, Pummerer reaction, sulfur, thionium ions, CYCLATIVE-CAPTURE STRATEGY, N-HETEROCYCLES, STEREOSELECTIVE-SYNTHESIS, OXIDATIVE CYCLIZATION, SULFOXIDE, REARRANGEMENT, DERIVATIVES, ANHYDRIDE, OXINDOLES, SULFIDE",
author = "Smith, {Laura H. S.} and Coote, {Susannah C.} and Sneddon, {Helen F.} and Procter, {David J.}",
year = "2010",
month = aug,
day = "9",
doi = "10.1002/anie.201000517",
language = "English",
volume = "49",
pages = "5832--5844",
journal = "Angewandte Chemie International Edition",
issn = "1433-7851",
publisher = "Wiley-VCH Verlag",
number = "34",

}

RIS

TY - JOUR

T1 - Beyond the Pummerer reaction

T2 - recent developments in Thionium ion chemistry

AU - Smith, Laura H. S.

AU - Coote, Susannah C.

AU - Sneddon, Helen F.

AU - Procter, David J.

PY - 2010/8/9

Y1 - 2010/8/9

N2 - Since the early 1960s the Pummerer reaction has evolved to become an indispensable tool for synthesis, and continues to serve as a source of inspiration for organic chemists. In recent years, many exciting advances have demonstrated the broad scope and synthetic utility of Pummerer methodology and the versatility of thionium ion intermediates.

AB - Since the early 1960s the Pummerer reaction has evolved to become an indispensable tool for synthesis, and continues to serve as a source of inspiration for organic chemists. In recent years, many exciting advances have demonstrated the broad scope and synthetic utility of Pummerer methodology and the versatility of thionium ion intermediates.

KW - cyclization

KW - heterocycles

KW - Pummerer reaction

KW - sulfur

KW - thionium ions

KW - CYCLATIVE-CAPTURE STRATEGY

KW - N-HETEROCYCLES

KW - STEREOSELECTIVE-SYNTHESIS

KW - OXIDATIVE CYCLIZATION

KW - SULFOXIDE

KW - REARRANGEMENT

KW - DERIVATIVES

KW - ANHYDRIDE

KW - OXINDOLES

KW - SULFIDE

U2 - 10.1002/anie.201000517

DO - 10.1002/anie.201000517

M3 - Literature review

VL - 49

SP - 5832

EP - 5844

JO - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

SN - 1433-7851

IS - 34

ER -