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dc.creatorMitch, Eugene L.
dc.date.accessioned 2007-08-21T01:05:10Z
dc.date.available 2007-08-21T01:05:10Z
dc.date.issued 1959
dc.identifier.urihttps://hdl.handle.net/1911/18371
dc.description.abstract A possible route for an unambiguous synthesis, and therefore proof of structure, of the 2-hydroxy-1-phenylindene-3-carboxylate (XXIX) might start with 1,4-dihydro-1-phenylnaphthalene (XLI) which on oxidative cleavage of the double bond should give rise to alpha-phenyl-o-benzenediacetic acid (XLII). Esterification of XLII followed by base catalyzed cyclization would be expected to give XXIX. It was the purpose of this research to carry out the indicated scheme as well as to investigate some novel approaches to the synthesis of XLI. The problem was successfully solved.
dc.format.mimetype application/pdf
dc.language.iso eng
dc.subjectOrganic chemistry
dc.title Part one. The synthesis of ethyl 1-phenyl-2-hydroxyindene-3-carboxylate. Part two. The anionic polymerization of 1,1-dicyanocyclopropane
dc.type.genre Thesis
dc.type.material Text
thesis.degree.department Chemistry
thesis.degree.discipline Natural Sciences
thesis.degree.grantor Rice University
thesis.degree.level Doctoral
thesis.degree.name Doctor of Philosophy
dc.identifier.citation Mitch, Eugene L.. "Part one. The synthesis of ethyl 1-phenyl-2-hydroxyindene-3-carboxylate. Part two. The anionic polymerization of 1,1-dicyanocyclopropane." (1959) Diss., Rice University. https://hdl.handle.net/1911/18371.


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