Stereoselective Synthesis of (±)-Ireland Alcohol Using Titanium-Mediated [2,3]Wittig Rearrangement Product as a Starting Material
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/65/7/65_7_1841/_pdf
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1. Recent Advances in the Total Synthesis of Tetramic Acid-Containing Natural Products;Journal of Chemistry;2016
2. Unified synthesis of tirandamycins and streptolydigins;Chemical Communications;2015
3. ChemInform Abstract: Stereoselective Synthesis of (.+-.)-Ireland Alcohol Using Titanium-Mediated (2,3)Wittig Rearrangement Product as a Starting Material.;ChemInform;2010-08-21
4. Asymmetric Epoxidation of Allylic Alcohols: the Katsuki-Sharpless Epoxidation Reaction;Organic Reactions;1996-03-12
5. One or More CH, CC, and/or CC Bonds Formed by Rearrangement;Comprehensive Organic Functional Group Transformations;1995
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