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Stereoisomeric Phytofluenes

Petracek, F. J. and Zechmeister, L. (1952) Stereoisomeric Phytofluenes. Journal of the American Chemical Society, 74 (1). pp. 184-186. ISSN 0002-7863. 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
Related URLs:
URLURL TypeDescription
https://doi.org/10.1021/ja01121a047DOIArticle
Additional Information:© 1952 American Chemical Society. Received June 19, 1951.
Other Numbering System:
Other Numbering System NameOther Numbering System ID
Gates and Crellin Laboratories of Chemistry1588
Issue or Number:1
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:03 Oct 2019 20:31

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