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  4. Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes

Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes

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Author(s)
Zhao, Yu
•
Hoveyda, Amir H.
•
Schrock, Richard Royce
Date Issued
January 2011
Journal
Organic Letters
Publisher
American Chemical Society
Citation
Zhao, Yu, Amir H. Hoveyda, and Richard R. Schrock. “Endo-Selective Enyne Ring-Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes.” Organic Letters 13.4 (2011): 784–787.
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Author's final manuscript
Abstract
The utility of W-alkylidene complexes for enyne ring-closing metathesis is demonstrated in a direct comparison with Mo-based analogs. Tungsten complexes lead to less alkyne oligomerization and higher levels of endo-selectivity and enantioselectivity.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
http://hdl.handle.net/1721.1/69936
DOI of Published Version
https://doi.org/10.1021/ol1030525
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