Literature DB >> 11317300

A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis This research was supported by the National Institutes of Health (GM-59426) and the National Science Foundation (CHE-9905806 to A. H. H. and CHE-9988766 to R. R. S.).

Sarah L. Aeilts1, Dustin R. Cefalo, Peter J. Bonitatebus, Jeffrey H. Houser, Amir H. Hoveyda, Richard R. Schrock.   

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Year:  2001        PMID： 11317300

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  3 in total

1.  Highly active chiral ruthenium catalysts for asymmetric ring-closing olefin metathesis.

Authors:  Timothy W Funk; Jacob M Berlin; Robert H Grubbs
Journal:  J Am Chem Soc       Date:  2006-02-15       Impact factor: 15.419

2.  Design and stereoselective preparation of a new class of chiral olefin metathesis catalysts and application to enantioselective synthesis of quebrachamine: catalyst development inspired by natural product synthesis.

Authors:  Elizabeth S Sattely; Simon J Meek; Steven J Malcolmson; Richard R Schrock; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2009-01-28       Impact factor: 15.419

3.  Evolution of catalytic stereoselective olefin metathesis: from ancillary transformation to purveyor of stereochemical identity.

Authors:  Amir H Hoveyda
Journal:  J Org Chem       Date:  2014-04-10       Impact factor: 4.354
  3 in total

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