Lewis Acid-Mediated Cycloaddition of Methylenecyclopropanes with Aldehydes and Imines: A Facile Access to Indene, THF, and Pyrrolidine Skeletons via Homoallylic Rearrangement Protocol-Reference-Cited by-同舟云学术

Lewis Acid-Mediated Cycloaddition of Methylenecyclopropanes with Aldehydes and Imines: A Facile Access to Indene, THF, and Pyrrolidine Skeletons via Homoallylic Rearrangement Protocol

Published:2004-03-04 Issue:7 Volume:6 Page:1175-1178
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shi Min¹,Xu Bo¹,Huang Jin-Wen¹

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0498242

Reference17 articles.

1. Transition Metal-Catalyzed Reactions of Methylenecyclopropanes

2. Novel [3+2] Cycloaddition of Alkylidenecyclopropanes with Aldehydes Catalyzed by Palladium

3. Palladium-catalyzed [3+2] cycloaddition of alkylidenecyclopropanes with imines

4. Palladium-Catalyzed Hydroalkoxylation of Methylenecyclopropanes

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