Jenny, Erwin F. and Roberts, John D. (1956) Small-Ring Compounds. XIII. The Mechanism of Racemization of Optically Active 2,4-Dichloro-3-phenylcyclobutenone. Journal of the American Chemical Society, 78 (9). pp. 2005-2009. ISSN 0002-7863. doi:10.1021/ja01590a068. https://resolver.caltech.edu/CaltechAUTHORS:20151021-112215086
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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.
Item Type: | Article | |||||||||
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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. | |||||||||
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Issue or Number: | 9 | |||||||||
DOI: | 10.1021/ja01590a068 | |||||||||
Record Number: | CaltechAUTHORS:20151021-112215086 | |||||||||
Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20151021-112215086 | |||||||||
Official Citation: | Small-Ring Compounds. XIII. The Mechanism of Racemization of Optically Active 2,4-Dichloro-3-phenylcyclobutenone Erwin F. Jenny and John D. Roberts Journal of the American Chemical Society 1956 78 (9), 2005-2009 DOI: 10.1021/ja01590a068 | |||||||||
Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | |||||||||
ID Code: | 61378 | |||||||||
Collection: | CaltechAUTHORS | |||||||||
Deposited By: | Ruth Sustaita | |||||||||
Deposited On: | 21 Oct 2015 20:06 | |||||||||
Last Modified: | 10 Nov 2021 22:48 |
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