Lewis Acid Assisted Ring-Closing Metathesis of Chiral Diallylamines: An Efficient Approach to Enantiopure Pyrrolidine Derivatives-Reference-Cited by-同舟云学术

Lewis Acid Assisted Ring-Closing Metathesis of Chiral Diallylamines: An Efficient Approach to Enantiopure Pyrrolidine Derivatives

Published:2005-01-28 Issue:5 Volume:7 Page:871-874
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yang Qian¹,Xiao Wen-Jing¹,Yu Zhengkun¹

Affiliation:

1. The Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China, and Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, Liaoning 116023, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol047356q

Reference43 articles.

1. Latent Ruthenium Olefin Metathesis Catalysts That Contain an N-Heterocyclic Carbene Ligand

2. Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts

3. Synthesis and metathesis reactions of a phosphine-free dihydroimidazole carbene ruthenium complex

4. Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands

5. Synthesis of Phosphorus and Sulfur Heterocycles via Ring-Closing Olefin Metathesis

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