Highly Stereoselective Synthesis of Trisubstituted Vinylcyclopropane Derivatives via Arsonium Ylides-Reference-Cited by-同舟云学术

Highly Stereoselective Synthesis of Trisubstituted Vinylcyclopropane Derivatives via Arsonium Ylides

Published:2005-11-01 Issue:24 Volume:70 Page:10202-10205
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jiang Hong¹,Deng Xianming¹,Sun Xiuli¹,Tang Yong¹,Dai Li-Xin¹

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, 354 Fenglin Lu, Shanghai 200032, China tangy@mail.sioc.ac.cn

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo051782n

Reference32 articles.

1. Enantioselective Addition of Nitrones to Activated Cyclopropanes

2. Highly Diastereoselective Synthesis of Tetrahydrofurans via Lewis Acid-Catalyzed Cyclopropane/Aldehyde Cycloadditions

3. Magnesium Iodide Promoted Reactions of Nitrones with Cyclopropanes: A Synthesis of Tetrahydro-1,2-oxazines

4. A Homo [3+2] Dipolar Cycloaddition: The Reaction of Nitrones with Cyclopropanes

5. Cyclopentannulation of 3-Alkylindoles: A Synthesis of a Tetracyclic Subunit of the Kopsane Alkaloids

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