Magnesium Bromide-PromotedE⁄Z-Isomerization of Carbonyl-Conjugated Nitrones and Highly Stereo- and Regioselective Cycloadditions to Allylic Alcohol Dipolarophiles-Reference-Cited by-同舟云学术

Magnesium Bromide-PromotedE⁄Z-Isomerization of Carbonyl-Conjugated Nitrones and Highly Stereo- and Regioselective Cycloadditions to Allylic Alcohol Dipolarophiles

Published:1995-01 Issue:1 Volume:24 Page:49-50
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Kanemasa Shuji,Tsuruoka Takashi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/24/1/24_1_49/_pdf

Reference10 articles.

1. Lewis acid-catalyzed nitrone cycloadditions to bidentate and tridentate α,β-unsaturated ketones. High rate acceleration, absolutely endo-selective and regioselective reactions

2. Metallic base-induced and Lewis acid-catalyzed nitrone cycloadditions to allyl alcohol dipolarophiles. Highly effective regio- and stereocontrol

3. One step bicyclization by way of tandem transesterification, intramolecular 1,3-dipolar cycloaddition of α-methoxycarbonylnitrones with allyl alcohols in the presence of titanium isopropoxide

4. The Configurations ofN-Methyl- andN-t-Butyl-α-methoxycarbonylmethanimineN-Oxides

5. Aromatic solvent-induced shifts in the 1H-NMR spectra of nitrones

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