Journal article

Photochemical alkene isomerization for the synthesis of polysubstituted furans and pyrroles under neutral conditions

Abstract:: A photochemical approach to polysubstituted heterocycles using UV‐induced alkene isomerization is described. The method allows for the synthesis of disubstituted furans and pyrroles under mild and neutral conditions and also provides access to a class of trisubstituted furans pertinent to natural‐product synthesis. The method has broad functional‐group tolerance and many richly decorated heterocycles have been prepared incorporating functional groups that are unstable under Brønsted and Lewis acidic conditions.

Publication status:: Published

Peer review status:: Peer reviewed

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APA Style

Walker, J., Werrel, S., & Donohoe, T. (2019). Photochemical alkene isomerization for the synthesis of polysubstituted furans and pyrroles under neutral conditions. Chemistry - A European Journal, 25(57), 13114–13118.

MLA Style

Walker, J, et al. “Photochemical Alkene Isomerization for the Synthesis of Polysubstituted Furans and Pyrroles under Neutral Conditions.” Chemistry - A European Journal, vol. 25, no. 57, 2019, pp. 13114–18.

Chicago Style

Walker, J, S Werrel, and T Donohoe. 2019. “Photochemical Alkene Isomerization for the Synthesis of Polysubstituted Furans and Pyrroles under Neutral Conditions.” Chemistry - A European Journal 25 (57): 13114–18.
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Files:: WalkeretalAAM2019

(Preview, Accepted manuscript, pdf, 1.1MB, Terms of use)

Publisher copy:: 10.1002/chem.201903590

Authors

+ Walker, J More by this author

Role:: Author

+ Werrel, S More by this author

Role:: Author

+ Donohoe, T More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Oxford college:: Magdalen College
Role:: Author

Publisher:: Wiley
Journal:: Chemistry - A European Journal More from this journal
Volume:: 25
Issue:: 57
Pages:: 13114-13118
Publication date:: 2019-08-07
Acceptance date:: 2019-08-07
DOI:: 10.1002/chem.201903590
EISSN:: 1521-3765
ISSN:: 0947-6539

Language:: English
Keywords:: FT
Pubs id:: pubs:1039338
UUID:: uuid:8f712a76-e7d8-4a8f-8f05-858c12c54f11
Local pid:: pubs:1039338
Source identifiers:: 1039338
Deposit date:: 2019-08-07
ARK identifier:: ark:/29072/ora_8f712a76e7d84a8f8f05858c12c54f11

Terms of use

Copyright holder:: Wiley
Copyright date:: 2019
Rights statement:: © 2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
Notes:: This is the accepted manuscript version of the article. The final version is available from Wiley at: https://doi.org/10.1002/chem.201903590

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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