Highly Substituted 2,3-Dihydroisoxazoles by Et3N-Catalyzed Tandem Reaction of Electron-Deficient 1,3-Conjugated Enynes with Hydroxylamines-Reference-Cited by-同舟云学术

Highly Substituted 2,3-Dihydroisoxazoles by Et3N-Catalyzed Tandem Reaction of Electron-Deficient 1,3-Conjugated Enynes with Hydroxylamines

Published:2010-03-24 Issue:8 Volume:12 Page:1876-1879
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yu Xiuzhao¹,Du Bo¹,Wang Kai¹,Zhang Junliang¹

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University, 3663 North Zhongshan Road, Shanghai 200062, P.R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol100490y

Reference67 articles.

1. .DELTA.4-Isoxazolines (2,3-dihydroisoxazoles)

2. Synthesis of stable Δ4-isoxazolines by 1,3-dipolar cycloaddition of 3,4-dihydroisoquinoline N-oxides with alkynes and their rearrangement to isoquinoline-fused pyrroles

3. 1,3-Dipolar cycloadditions of nitrones derived from the reaction of acetylenes with hydroxylamines

4. Peracid oxidation of 4-isoxazolines as a method for the preparation of .alpha.,.beta.-unsaturated carbonyl compounds

5. Tandem [3+2]-cycloaddition [2,3]-sigmatropic rearrangement reaction of allenyl sulfoxides with nitrones

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