Published May 1, 1960
| public
Journal Article
Small-Ring Compounds. XXVIII. Isotope-Position Rearrangements of Allylcarbinyl Grignard Reagents
Abstract
We have observed a remarkable rearrangement while attempting to prepare 4-penten-2-ylarnine (I) through the reaction of the Grignard reagent derived from 4-penten-2-yl chloride (II) with methoxylamine, in that part of the amine formed appeared to be 2-methyl-3-butenylamine (III).
Additional Information
© 1960 American Chemical Society. Received April 9, 1960. Supported in part by the Office of Naval Research and the Petroleum Research Fund of the American Chemical Society. Grateful acknowledgment is hereby made to the donors of the Petroleum Research Fund. Presented in part at the Sixteenth National Organic Symposium, Seattle, Washington, June 15, 1959.Additional details
- Eprint ID
- 61335
- DOI
- 10.1021/ja01495a068
- Resolver ID
- CaltechAUTHORS:20151020-124117005
- Office of Naval Research (ONR)
- American Chemical Society Petroleum Research Fund
- 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
- 2570