Published April 1, 1961
| public
Journal Article
Small-Ring Compounds. XXXIII. A Study by Nuclear Magnetic Resonance of the Extent of Isotope-position Rearrangement in the Vapor-phase Photochlorination of methyl-^(13)C-Cyclopropane
Chicago
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Abstract
Vapor-phase photochlorination of methyl-^(13)C-cyclopropane was found to yield cyclopropylcarbinyl-α-^(13)C chloride and allyl-γ-^(13)C-carbinyl chloride. Within the experimental error of the analytical method (nuclear magnetic resonance spectroscopy), no other ^(13)C-position isomers of the chlorides were formed.
Additional Information
© 1961 American Chemical Society. Received December 14, 1960. Supported in part by the Office of Naval Research, 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 Faculty Fellow, 1959-1960.Additional details
- Eprint ID
- 61324
- DOI
- 10.1021/ja01469a049
- Resolver ID
- CaltechAUTHORS:20151020-105558215
- Office of Naval Research (ONR)
- American Chemical Society Petroleum Research Fund
- NSF
- Created
-
2015-10-20Created 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
- 2646