1,3-Dipolar cycloaddition of α-alkoxycarbonylnitrones with vinyl ethers and allyl alcohols in the presence of Eu(fod)3: selective activation of (Z)-isomers of the nitrones-Reference-Cited by-同舟云学术

1,3-Dipolar cycloaddition of α-alkoxycarbonylnitrones with vinyl ethers and allyl alcohols in the presence of Eu(fod)3: selective activation of (Z)-isomers of the nitrones

Published:2006-12 Issue:52 Volume:62 Page:12227-12236
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tamura Osamu,Mita Naka,Imai Yasuharu,Nishimura Takuya,Kiyotani Tamiko,Yamasaki Mikio,Shiro Motoo,Morita Nobuyoshi,Okamoto Iwao,Takeya Tetsuya,Ishibashi Hiroyuki,Sakamoto Masanori

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference89 articles.

1. For general reviews on cycloadditions of nitrones, see:

2. Optically active isoxazolidines via asymmetric cycloaddition reactions of nitrones with alkenes: applications in organic synthesis

3. Asymmetric 1,3-Dipolar Cycloaddition Reactions

4. 1,3-Dipolar cycloaddition reactions of carbohydrate derived nitrones and oximes

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