Petracek, F. J. and Zechmeister, L. (1952) Stereoisomeric Phytofluenes. Journal of the American Chemical Society, 74 (1). pp. 184-186. ISSN 0002-7863. doi:10.1021/ja01121a047. https://resolver.caltech.edu/CaltechAUTHORS:20181120-153101373
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Abstract
Phytofluene ex tomatoes is subject to cis-trans isomerization. The native form in the tomatoes studied is a relatively thermostable but photosensitive cis compound that may rearrange spontaneously or when illuminated or under the catalytic influence of iodine in light. It then yields the more stable all-trans form possessing stronger adsorbability. The two main stereoisomers mentioned were characterized by spectroscopic and chromatographic methods.
| Item Type: | Article | ||||||
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| Additional Information: | © 1952 American Chemical Society. Received June 19, 1951. | ||||||
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| Issue or Number: | 1 | ||||||
| DOI: | 10.1021/ja01121a047 | ||||||
| Record Number: | CaltechAUTHORS:20181120-153101373 | ||||||
| Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20181120-153101373 | ||||||
| Official Citation: | Stereoisomeric Phytofluenes F. J. Petracek and L. Zechmeister Journal of the American Chemical Society 1952 74 (1), 184-186 DOI: 10.1021/ja01121a047 | ||||||
| Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | ||||||
| ID Code: | 91113 | ||||||
| Collection: | CaltechAUTHORS | ||||||
| Deposited By: | George Porter | ||||||
| Deposited On: | 21 Nov 2018 18:54 | ||||||
| Last Modified: | 16 Nov 2021 03:38 |
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