Journal article

Cu-catalyzed asymmetric addition of sp2-hybridized zirconium nucleophiles to racemic allyl bromides

Abstract:: Alkenylzirconium nucleophiles made in situ by the hydrozirconation of terminal alkynes undergo dynamic kinetic asymmetric allylic alkenylation with racemic allyl bromides to give enantioenriched products.

Publication status:: Published

Peer review status:: Peer reviewed

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APA Style

Sidera, M., & Fletcher, S. (2015). Cu-catalyzed asymmetric addition of sp2-hybridized zirconium nucleophiles to racemic allyl bromides. Chemical Communications, 51(24), 5044–5047.

MLA Style

Sidera, M, and S Fletcher. “Cu-Catalyzed Asymmetric Addition of sp2-Hybridized Zirconium Nucleophiles to Racemic Allyl Bromides.” Chemical Communications, vol. 51, no. 24, 2015, pp. 5044–47.

Chicago Style

Sidera, M, and S Fletcher. 2015. “Cu-Catalyzed Asymmetric Addition of sp2-Hybridized Zirconium Nucleophiles to Racemic Allyl Bromides.” Chemical Communications 51 (24): 5044–47.
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Publisher copy:: 10.1039/c5cc00421g

Publication website:: http://pubs.rsc.org/en/Content/ArticleLanding/2015/CC/c5cc00421g

Authors

+ Sidera, M More by this author

Department:: University of Oxford
Role:: Author

+ Fletcher, S More by this author

Department:: University of Oxford
Role:: Author

+ Engineering and Physical Sciences Research Council More from this funder

Grant:: D4DND4A1.DPA1.3

Publisher:: Royal Society of Chemistry
Journal:: Chemical Communications More from this journal
Volume:: 51
Issue:: 24
Pages:: 5044-5047
Publication date:: 2015-02-23
Acceptance date:: 2015-02-13
DOI:: 10.1039/c5cc00421g
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
UUID:: uuid:764be43c-532f-4bde-a740-b9e6519ff4c3
Deposit date:: 2015-09-15
ARK identifier:: ark:/29072/ora_764be43c532f4bdea740b9e6519ff4c3

Terms of use

Copyright date:: 2015

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

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