Sodium Bis(trimethylsilyl)amide and Lithium Diisopropylamide in Deprotection of Alkyl Aryl Ethers: α-Effect of Silicon
Author:
Affiliation:
1. Organosilicon and Synthesis Laboratory, Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan 30043, Republic of China, and Institute of Chemistry, Academia Sinica, Nankang, Taipei, Taiwan 11529, Republic of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo961191k
Reference44 articles.
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2. Fieser, F.; Fieser, L. F.Reagents for Organic Synthesis; John Wiley: New York, 1967; Vol. 1, p 1046.
3. The trimethylsilyl cationic species as a bulky proton. Application to chemoselective dioxolanation
4. Calcium in liquid ammonia for the reduction of benzyl ethers. Mechanistic clues derived from chemoselectivity studies
5. General scope of 1,3-dioxolanation of .alpha.,.beta.-unsaturated aldehydes with 1,2-bis(trimethylsilyloxy)ethane and trimethylsilyl trifluoromethanesulfonate
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