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  An experimental and theoretical study of stereoselectivity of furan-maleic anhydride and furan-maleimide Diels-Alder reactions

Rulisek, L., Sebek, P., Havlas, Z., Hrabal, R., Capek, P., & Svatos, A. (2005). An experimental and theoretical study of stereoselectivity of furan-maleic anhydride and furan-maleimide Diels-Alder reactions. Journal of Organic Chemistry, 70(16), 6295-6302.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0012-B410-D Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0012-B411-B
Genre: Journal Article

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MS049.pdf (Publisher version), 0B
 
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 Creators:
Rulisek, L., Author
Sebek, P., Author
Havlas, Z., Author
Hrabal, R., Author
Capek, P., Author
Svatos, A.1, Author              
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1Research Group Mass Spectrometry, MPI for Chemical Ecology, Max Planck Society, ou_421899              

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Free keywords: Secondary orbital interactions Density-functional theory Ab-initio Stepwise mechanisms Multiresponse data High-pressure Basis sets Molecules Cycloaddition Cyclopentadiene. Chemistry & Analysis in Current Contents(R)/Life Sciences. Organic Chemistry/Polymer Science in Current Contents(R)/Physical, Chemical & Earth Sciences.
 Abstract: The stereoselectivity of the reaction of furan (1) with maleic anhydride (2) and maleimide (3) was studied experimentally and theoretically. Although the two reactions are highly similar with regard to their preference for endo and exo steroisomers, not

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 Dates: 2005
 Publication Status: Published in print
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 Identifiers: Other: MS049
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Title: Journal of Organic Chemistry
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Source Genre: Journal
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Pages: - Volume / Issue: 70 (16) Sequence Number: - Start / End Page: 6295 - 6302 Identifier: -