Grohmann, K. and Grutzner, J .B. and Roberts, John D. (1969) Nuclear magnetic resonance spectroscopy ^(13)C Spectrum of a Dimer of Cyclooatatetraene. Tetrahedron Letters, 10 (12). pp. 917-918. ISSN 0040-4039. https://resolver.caltech.edu/CaltechAUTHORS:20151026-093705693
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Abstract
The structure of the cyclooctatetraene dimer of m. p. 53° has been a matter of controversy. Structure I was proposed by Jones(3} and could be reconciled with a proposed mechanism of conversion of the dimer to bullvalene(4). Schröder(5) has proposed structure II because the material afforded the all cis-cyclobutanetetracarboxylic acid on ozonolysis and peracid oxidation. However, there is still a possibility that I could yield ciclobutanetetracarboxilic acid on oxidation by way of its valence tautomer III.
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| Additional Information: | © 1969 Pergamon Press. Received in USA. 27 January 1969; received in UK for publication 6 February 1969. Supported by the National Science Foundation and USPHS Research Grant 11072-06 from the Division of Medical Sciences. Contribution No. 3801. | |||||||||
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| Issue or Number: | 12 | |||||||||
| Record Number: | CaltechAUTHORS:20151026-093705693 | |||||||||
| Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20151026-093705693 | |||||||||
| Official Citation: | K. Grohmann, J.B. Grutzner, John D. Roberts, Nuclear magnetic resonance spectroscopy : 13C spectrum of a dimer of cyclooctatetraene(1), Tetrahedron Letters, Volume 10, Issue 12, 1969, Pages 917-918, ISSN 0040-4039, http://dx.doi.org/10.1016/S0040-4039(01)97697-X. (http://www.sciencedirect.com/science/article/pii/S004040390197697X) | |||||||||
| Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | |||||||||
| ID Code: | 61519 | |||||||||
| Collection: | CaltechAUTHORS | |||||||||
| Deposited By: | Ruth Sustaita | |||||||||
| Deposited On: | 26 Oct 2015 21:58 | |||||||||
| Last Modified: | 03 Oct 2019 09:08 |
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