Published May 1, 1956
| Version public
Journal Article
Small-Ring Compounds. XIII. The Mechanism of Racemization of Optically Active 2,4-Dichloro-3-phenylcyclobutenone
Creators
Abstract
Racemization of optically active 2,4-dichloro-3-phenylcyclobutenone has been shown to involve reversible formation of (1-phenyl-2-chloroethenyl)-chloroketene 2,4-dichloro-3-phenyl-3-butenoic acid yields 2,4-dichloro-3-phenylcyclobutenone on treatment with acetic anhydride.
Additional Information
© 1956 American Chemical Society. Received August 29, 1955. Presented at the 14th National Organic Symposium of the American Chemical Society, Lafayette, Ind, June 14, 1955. Arthur Amos Noyes Fellow, 1954-1955.Additional details
Identifiers
- Eprint ID
- 61378
- Resolver ID
- CaltechAUTHORS:20151021-112215086
Funding
- Caltech Arthur A. Noyes Fellowship
Dates
- Created
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2015-10-21Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field
Caltech Custom Metadata
- Other Numbering System Name
- Caltech Gates and Crellin Laboratories of Chemistry
- Other Numbering System Identifier
- 2029