Highly Stereoselective Synthesis of Trisubstituted Vinylcyclopropane Derivatives via Arsonium Ylides
Author:
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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3. Stereocontrolled Synthesis of trans/cis-2,3-Disubstituted Cyclopropane-1,1-diesters and Applications in the Syntheses of Furanolignans;The Journal of Organic Chemistry;2018-09-17
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