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Graphical Abstract: Asian J. Org. Chem. 1/2015

Graphical Abstract: Asian J. Org. Chem. 1/2015 Contents FEATURED ARTICLES 3-Alkyloxycyclobutanones are highly reactive due to the strain energy in the cyclobutane ring. They also form zwitterionic intermediates in the presence of Lewis-acid catalysts, which makes them highly suitable for cycloaddition reactions. In their Focus Review on page 16, Yu Rao and co-workers discuss synthetic approaches to 3-ethoxycyclobutanones and the applications of these compounds and their derivatives, especially in formal [4+2], [3+2], and [3+3] annulations. FOCUS REVIEWS Heterocycles Shi Chen, Gang Shan, Pengju Nie, Yu Rao* .................................. 16 – 26 3-Alkyloxycyclobutanones as Useful Synthons for Heterocycle and Be there and square: Substituted 3- Lewis acid catalysis, 3-alkyloxycyclobuta- Carbocycle Synthesis alkyloxycyclobutanones are highly val- nones can form zwitterionic intermedi- uable intermediates in organic synthe- ates and participate in a series of cyclo- sis, which demonstrate interesting and addition reactions as three- or four- rich reactivity in different types of reac- carbon synthons. tions due to the strain energy. Under COMMUNICATIONS Cycloaddition Wen-Ke Li, Ze-Shui Liu, Long He,* Tai-Ran Kang,* Quan-Zhong Liu* . 28 – 32 Enantioselective Cycloadditions of Vinyl Cyclopropanes and Nitroolefins for Functionally and Optically Enriched Nitrocyclopentanes Spinning the vinyl: Palladium catalyzed nitroolefins were realized for construct- enantioselective (3+2) cycloadditions of ing structurally and optically enriched http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

Graphical Abstract: Asian J. Org. Chem. 1/2015

Asian Journal of Organic Chemistry , Volume 4 (1) – Jan 1, 2015
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Publisher
Wiley
Copyright
Copyright © 2015 Wiley Subscription Services, Inc., A Wiley Company
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201590001
Publisher site
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Abstract

Contents FEATURED ARTICLES 3-Alkyloxycyclobutanones are highly reactive due to the strain energy in the cyclobutane ring. They also form zwitterionic intermediates in the presence of Lewis-acid catalysts, which makes them highly suitable for cycloaddition reactions. In their Focus Review on page 16, Yu Rao and co-workers discuss synthetic approaches to 3-ethoxycyclobutanones and the applications of these compounds and their derivatives, especially in formal [4+2], [3+2], and [3+3] annulations. FOCUS REVIEWS Heterocycles Shi Chen, Gang Shan, Pengju Nie, Yu Rao* .................................. 16 – 26 3-Alkyloxycyclobutanones as Useful Synthons for Heterocycle and Be there and square: Substituted 3- Lewis acid catalysis, 3-alkyloxycyclobuta- Carbocycle Synthesis alkyloxycyclobutanones are highly val- nones can form zwitterionic intermedi- uable intermediates in organic synthe- ates and participate in a series of cyclo- sis, which demonstrate interesting and addition reactions as three- or four- rich reactivity in different types of reac- carbon synthons. tions due to the strain energy. Under COMMUNICATIONS Cycloaddition Wen-Ke Li, Ze-Shui Liu, Long He,* Tai-Ran Kang,* Quan-Zhong Liu* . 28 – 32 Enantioselective Cycloadditions of Vinyl Cyclopropanes and Nitroolefins for Functionally and Optically Enriched Nitrocyclopentanes Spinning the vinyl: Palladium catalyzed nitroolefins were realized for construct- enantioselective (3+2) cycloadditions of ing structurally and optically enriched

Journal

Asian Journal of Organic Chemistry – Wiley

Published: Jan 1, 2015

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