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

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.

Bibliographic Details
Main Authors: Zhao, Yu, Hoveyda, Amir H., Schrock, Richard Royce
Other Authors: Massachusetts Institute of Technology. Department of Chemistry
Format: Article
Language:en_US
Published: American Chemical Society 2012
Online Access:http://hdl.handle.net/1721.1/69936
https://orcid.org/0000-0001-5827-3552
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author Zhao, Yu
Hoveyda, Amir H.
Schrock, Richard Royce
author2 Massachusetts Institute of Technology. Department of Chemistry
author_facet Massachusetts Institute of Technology. Department of Chemistry
Zhao, Yu
Hoveyda, Amir H.
Schrock, Richard Royce
author_sort Zhao, Yu
collection MIT
description 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.
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spelling mit-1721.1/699362022-10-01T08:06:29Z Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes Zhao, Yu Hoveyda, Amir H. Schrock, Richard Royce Massachusetts Institute of Technology. Department of Chemistry Schrock, Richard Royce Schrock, Richard Royce Zhao, Yu 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. National Institutes of Health (U.S.) (GM-59426) 2012-04-04T20:00:34Z 2012-04-04T20:00:34Z 2011-01 2010-12 Article http://purl.org/eprint/type/JournalArticle 1523-7060 1523-7052 http://hdl.handle.net/1721.1/69936 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. https://orcid.org/0000-0001-5827-3552 en_US http://dx.doi.org/10.1021/ol1030525 Organic Letters 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. application/pdf American Chemical Society Prof. Schrock via Erja Kajosalo
spellingShingle Zhao, Yu
Hoveyda, Amir H.
Schrock, Richard Royce
Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes
title Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes
title_full Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes
title_fullStr Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes
title_full_unstemmed Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes
title_short Endo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes
title_sort endo selective enyne ring closing metathesis promoted by stereogenic at w mono pyrrolide complexes
url http://hdl.handle.net/1721.1/69936
https://orcid.org/0000-0001-5827-3552
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AT schrockrichardroyce endoselectiveenyneringclosingmetathesispromotedbystereogenicatwmonopyrrolidecomplexes