Chem. Commun., 2012, Advance Article
DOI: 10.1039/C2CC34619B, Communication
DOI: 10.1039/C2CC34619B, Communication
Xiao-nan Zhang, Hong-Ping Deng, Long Huang, Yin Wei, Min Shi
A novel asymmetric [4+1] cycloaddition of MBH carbonates with dicyano-2-methylenebut-3-enoates has been developed for the first time, providing an efficient and enantioselective synthesis of highly functionalized cyclopentenes bearing one all-carbon quaternary stereogenic center.
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A novel asymmetric [4+1] cycloaddition of MBH carbonates with dicyano-2-methylenebut-3-enoates has been developed for the first time, providing an efficient and enantioselective synthesis of highly functionalized cyclopentenes bearing one all-carbon quaternary stereogenic center.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry
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