An Experimental and Theoretical Study of Stereoselectivity of Furan−Maleic Anhydride and Furan−Maleimide Diels−Alder Reactions-Reference-Cited by-同舟云学术

An Experimental and Theoretical Study of Stereoselectivity of Furan−Maleic Anhydride and Furan−Maleimide Diels−Alder Reactions

Published:2005-07-12 Issue:16 Volume:70 Page:6295-6302
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Rulíšek Lubomír¹,Šebek Pavel¹,Havlas Zdeněk¹,Hrabal Richard¹,Čapek Pavel¹,Svatoš Aleš¹

Affiliation:

1. Max-Planck-Institute for Chemical Ecology, Hans-Knöll-Str. 8, 07745, Jena, Germany, Institute of Organic Chemistry and Biochemistry and Center for Complex Molecular Systems and Biomolecules, Academy of Sciences of the Czech Republic Flemingovo náměstí 2, 166 10 Prague 6, Czech Republic, and Laboratory of NMR Spectroscopy and Department of Organic Technology, Prague Institute of Chemical Technology, Technická 5, Prague 6, Zentiva a.s., U Kabelovny 130, Prague 10, Czech Republic

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo050759z

Reference44 articles.

1. Orbital Symmetries and endo-exo Relationships in Concerted Cycloaddition Reactions

2. Mechanistic Aspects of Diels-Alder Reactions: A Critical Survey

3. Endo preference in the Diels-Alder cycloaddition of butadiene and maleic anhydride

4. Recognition-induced control of a Diels-Alder cycloaddition

5. Retro Diels−Alder Reactions of 5,6-Disubstituted-7-oxabicyclo[2.2.1]hept-2-enes: Experimental and Density Functional Theory Studies

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