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dc.contributor.authorZhao, Yu
dc.contributor.authorHoveyda, Amir H.
dc.contributor.authorSchrock, Richard Royce
dc.date.accessioned2012-04-04T20:00:34Z
dc.date.available2012-04-04T20:00:34Z
dc.date.issued2011-01
dc.date.submitted2010-12
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.urihttp://hdl.handle.net/1721.1/69936
dc.description.abstractThe 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.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (GM-59426)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol1030525en_US
dc.rightsArticle 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.en_US
dc.sourceProf. Schrock via Erja Kajosaloen_US
dc.titleEndo-Selective Enyne Ring- Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexesen_US
dc.typeArticleen_US
dc.identifier.citationZhao, 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.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverSchrock, Richard Royce
dc.contributor.mitauthorSchrock, Richard Royce
dc.contributor.mitauthorZhao, Yu
dc.relation.journalOrganic Lettersen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsZhao, Yu; Hoveyda, Amir H.; Schrock, Richard R.en
dc.identifier.orcidhttps://orcid.org/0000-0001-5827-3552
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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