Published June 1, 1965
| public
Journal Article
Mechanism of the Diels-Alder Reaction. The Question of the "Internal" Pathway for the Thermal endo-exo Isomerizations of the 5-Norbornene-2,3-dicarboxylic Anhydrides
Abstract
Much information bearing on the mechanism of the Diels-Alder reaction has been obtained from studies of isomerizations of various adducts of cyclopentadiene. One of the most interesting and important of these isomerizations is the conversion of the endocyclopentadiene-maleic anhydride adduct [5-norbornene-2,3-endo-dicarboxylic anhydride (N)12] to the corresponding exo isomer (X) at 190º.
Additional Information
© 1965 American Chemical Society. Received April 28, 1965. Supported in part by the National Science Foundation.Additional details
- Eprint ID
- 61157
- Resolver ID
- CaltechAUTHORS:20151015-104906727
- NSF
- Created
-
2015-10-15Created from EPrint's datestamp field
- Updated
-
2021-11-10Created from EPrint's last_modified field
- Other Numbering System Name
- Caltech Gates and Crellin Laboratories of Chemistry
- Other Numbering System Identifier
- 3222