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-Reference-Cited by-同舟云学术

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

Published:2008-12-29 Issue:3 Volume:131 Page:943-953
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Sattely Elizabeth S.¹,Meek Simon J.¹,Malcolmson Steven J.¹,Schrock Richard R.¹,Hoveyda Amir H.¹

Affiliation:

1. Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, and Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja8084934

Reference109 articles.

1. Handbook of Metathesis

2. The remarkable metal-catalysed olefin metathesis reaction

3. Molybdenum and Tungsten Imido Alkylidene Complexes as Efficient Olefin-Metathesis Catalysts

4. The Total Synthesis of dl-Aspidospermine and of dl-Quebrachamine

5. A QUEBRACHAMINE MODEL

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