Efficient Stereoselective Synthesis of Nitrocyclopropanes by the Oxidative Cyclization of Michael Adducts of Nitroolefins with Activated Methylene Compounds-Reference-Cited by-同舟云学术

Efficient Stereoselective Synthesis of Nitrocyclopropanes by the Oxidative Cyclization of Michael Adducts of Nitroolefins with Activated Methylene Compounds

Published:2008-11-03 Issue:16 Volume:350 Page:2488-2492
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Fan Renhua,Ye Yang,Li Weixun,Wang Lingfei

Publisher

Wiley

Subject

General Chemistry

Reference110 articles.

1. Ring opening of 1,1-dinitrocyclopropane by addition of C, N, O and S nucleophiles

2. An Expedient and Practical Method for the Synthesis of a Diverse Series of Cyclopropane α-Amino Acids and Amines

3. Photoelectron Spectra and Electronic Structures of Some Acceptor-Substituted Cyclopropanes: Linear Correlation of Substituent Effects on MO Energies with Molecular Structures

4. Productive Asymmetric Synthesis of All Four Diastereomers of 3-(trans-2-Nitrocyclopropyl)alanine from Glycine with (S)- or (R)-2-[(N-Benzylprolyl)amino]benzophenone as a Reusable Chiral Auxiliary

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