Lewis Acid-catalyzed [3 + 2]Cyclo-addition of Alkynes withN-Tosyl-aziridines via Carbon–Carbon Bond Cleavage: Synthesis of Highly Substituted 3-Pyrrolines-Reference-Cited by-同舟云学术

Lewis Acid-catalyzed [3 + 2]Cyclo-addition of Alkynes withN-Tosyl-aziridines via Carbon–Carbon Bond Cleavage: Synthesis of Highly Substituted 3-Pyrrolines

Published:2011-10-26 Issue:22 Volume:13 Page:5940-5943
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Lei¹,Zhang Junliang¹²

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University, 3663 N. Zhongshan Road, Shanghai 200062 P.R. China

2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P.R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol202603e

Reference87 articles.

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3. An approach to 2,3-dihydropyrroles and β-iodopyrroles based on 5-endo-dig cyclisations

4. The Role of Natural Product Chemistry in Drug Discovery

5. Optimization of Novel Acyl Pyrrolidine Inhibitors of Hepatitis C Virus RNA-Dependent RNA Polymerase Leading to a Development Candidate

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