Kinetic Resolution of Secondary 2-Aryl-1-cycloalkanols with Phosphoroselenoyl Chloride with a Binaphthyl Group
Author:
Affiliation:
1. Department of Chemistry and Biomolecular Science; Faculty of Engineering, Gifu University; Yanagido Gifu 501-1193 Japan
2. JST, 4-1-8, Honcho; Kawaguchi Saitama 332-0012 Japan
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/hc.21168/fullpdf
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1. 4‐Chloro‐(11b)‐dinaphtho[2,1‐d:1′,2′‐f][1,3,2]dioxaphosphepin‐4‐selenide;Encyclopedia of Reagents for Organic Synthesis;2024-07-17
2. Axis-to-Center Chirality Transfer Reactions of Phosphates with a Binaphthyl Group and Their Congeners: New Synthetic Routes to P-Chirogenic Organophosphorus Compounds;Chemistry Letters;2023-08-01
3. Synthesis and Applications of Organophosphorus Compounds with a PSe Group;Chalcogen Chemistry: Fundamentals and Applications;2023-02-15
4. Synthetic Chemistry of Phosphoroselenoic Acid Derivatives with a Binaphthyl Group;Journal of Synthetic Organic Chemistry, Japan;2023-02-01
5. Discrimination of remote chirality of primary alcohols using 1,1′-binaphthyl-2,2′-DIYL phosphoroselenoyl chlorides as a chiral molecular tool;Phosphorus, Sulfur, and Silicon and the Related Elements;2016-02-01
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