A Highly Site-, Regio-, and Stereoselective Lewis Acid Catalyzed Formal [3+3] Cycloaddition of Methylenecyclopropane-1,1-Diesters with C,N-Diarylnitrones-Reference-Cited by-同舟云学术

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A Highly Site-, Regio-, and Stereoselective Lewis Acid Catalyzed Formal [3+3] Cycloaddition of Methylenecyclopropane-1,1-Diesters with C,N-Diarylnitrones

Published:2008-11-25 Issue:2 Volume:15 Page:324-327
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Hu Bao,Zhu Jianlin,Xing Siyang,Fang Jie,Du Ding,Wang Zhongwen

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.200801990/fullpdf

Reference92 articles.

1. Synthesis of Methylene- and Alkylidenecyclopropane Derivatives

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1. Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions;Russian Chemical Bulletin;2022-04

2. 1,2-Oxazines and Their Benzo Derivatives;Comprehensive Heterocyclic Chemistry IV;2022

3. Magnesium Halide‐Catalyzed Synthesis of Oxaspiro[2.5]octenes from a Methylenecyclopropane and Acyl Cyanoalkenes;European Journal of Organic Chemistry;2021-05-20

4. Palladium(II)‐Catalyzed Intermolecular Cascade Cyclization of Methylenecyclopropanes with Aromatic Alkynes: Construction of Spirocyclic Compounds Containing Indene and 1,2‐Dihydronaphthalene Moieties;Advanced Synthesis & Catalysis;2019-05-13

5. Gold(I)-Catalyzed Cycloisomerization of ortho -(Propargyloxy)arenemethylenecyclopropanes Controlled by Adjacent Substituents at Aromatic Rings;Chemistry - A European Journal;2017-05-08

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