Synthesis of γ‐Substituted‐β‐(Ethoxycarbonyl)allylsilanes via Peterson Olefination
Author:
Affiliation:
1. a Department of Chemistry , Rikkyo University , Nishi‐Ikebukuro, Toshima‐ku, Tokyo, 171‐8501, Japan
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/SCC-120030687
Reference23 articles.
1. Synthesis of Odd-membered Rings by the Reaction of β-Carbonylallylsilane or its Derivative as a Carbon 1,3-Dipole
2. Intramolecular cycloaddition reactions of allylic cations
3. Exploration of Fundamental and Synthetic Aspects of the Intramolecular 4 + 3 Cycloaddition Reaction
4. Synthesis of eleven-membered carbocycles via a homo-Cope type of five-carbon ring expansion reaction utilized β-(hydroxymethyl)allylsilane
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1. (Iodomethyl)trimethylsilane;Encyclopedia of Reagents for Organic Synthesis;2014-05-27
2. 2.02 Allylsilanes, Allylstannanes, and Related Compounds;Comprehensive Organic Synthesis II;2014
3. (Iodomethyl)trimethylsilane;Encyclopedia of Reagents for Organic Synthesis;2012-03-15
4. Peterson Olefination;Comprehensive Organic Name Reactions and Reagents;2010-09-15
5. Correlation of Hydrolysis and Desilylation of 2-[(Trimethylsilyl)methyl]acrylate Derivatives in Aqueous Alkali Solutions;Helvetica Chimica Acta;2008-05
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