Published January 1962
| public
Journal Article
Small-Ring Compounds. XXXVII. Free Radical Decarbonylation of Some Cyclopropanecarboxaldehydes
- Creators
-
Schuster, David I.
- Roberts, John D.
Abstract
The di-t-butyl peroxide initiated decarbonylations of cyclopropanecarboxaldehyde and 1-methyl- and 1-phenylcyclopropanecarboxaldehyde have been studied. The first of these did not undergo decerbonylation to a measurable extent, while the substituted aldehydes reacted without ring opening to give methyl- and phenylcyclopropane, respectively.
Additional Information
© 1962 American Chemical Society. Received August 2, 1961. Supported in part by the Petroleum Research Fund of the American Chemical Society and the National Science Foundation. Grateful acknowledgment is hereby made to the Donors of the Petroleum Research Fund. National Science Foundation Predoctoral Fellow 1956-1960.Additional details
- Eprint ID
- 61221
- Resolver ID
- CaltechAUTHORS:20151016-143424455
- American Chemical Society Petroleum Research Fund
- NSF
- NSF Predoctoral Fellowship
- Created
-
2015-10-16Created 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
- 2735