Exo Selective Cycloaddition Reactions of α-Hydroxy Cyclic Nitronates to Allylic Alcohols in the Presence of Magnesium Ions Leading to Isoxazolidines and Isoxazolines-Reference-Cited by-同舟云学术

Exo Selective Cycloaddition Reactions of α-Hydroxy Cyclic Nitronates to Allylic Alcohols in the Presence of Magnesium Ions Leading to Isoxazolidines and Isoxazolines

Published:2008-02-05 Issue:2 Volume:37 Page:146-147
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Nishiuchi Masaki,Sato Hiroyasu,Umemoto Nao,Murakami Sayoko

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference23 articles.

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2. Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions

3. First Successful Metal Coordination Control in 1,3-Dipolar Cycloadditions. High-Rate Acceleration and Regio- and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols

4. A highly effective quenching method of 1,3-dipolar cycloadditions of nitrile oxides or nitrile oxide/Lewis acid complexes by use of 2-propenyloxymagnesium bromide

5. Regiocontrol of nitrile oxide cycloadditions to allyl alcohols. Synthesis of 4-substituted and 4,4-disubstituted 5-hydroxymethyl-2-isoxazolines

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