Journal article

Substituted pyrroles via olefin cross-metathesis.

Abstract:: Olefin cross-metathesis (CM) provides a short and convenient entry to diverse trans-γ-aminoenones. When exposed to either acid or Heck arylation conditions, these intermediates are converted to mono-, di-, or trisubstituted pyrroles. The value of this chemistry is demonstrated by its application to the tetrasubstituted pyrrole subunit of Atorvastatin.

Publication status:: Published

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APA Style

Donohoe, T., Race, N., Bower, J., & Callens, C. (2010). Substituted pyrroles via olefin cross-metathesis. Organic Letters, 12(18), 4094–4097.

MLA Style

Donohoe, T., et al. “Substituted Pyrroles via Olefin Cross-Metathesis.” Organic Letters, vol. 12, no. 18, 2010, pp. 4094–97.

Chicago Style

Donohoe, T, N Race, J Bower, and C Callens. 2010. “Substituted Pyrroles via Olefin Cross-Metathesis.” Organic Letters 12 (18): 4094–97.
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Publisher copy:: 10.1021/ol101681r

Authors

+ Donohoe, T More by this author

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

+ Race, N More by this author

Role:: Author

+ Bower, J More by this author

Role:: Author

+ Callens, C More by this author

Role:: Author

Journal:: Organic letters More from this journal
Volume:: 12
Issue:: 18
Pages:: 4094-4097
Publication date:: 2010-09-01
DOI:: 10.1021/ol101681r
EISSN:: 1523-7052
ISSN:: 1523-7060

Language:: English
Pubs id:: pubs:67461
UUID:: uuid:873418f7-3406-493b-8e27-31257bf8c02a
Local pid:: pubs:67461
Source identifiers:: 67461
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2010

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

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