Show simple item record

dc.creatorWatson, WH
dc.creatorMarchand, AP
dc.creatorSivappa, R
dc.date.accessioned2022-01-31T17:27:28Z
dc.date.available2022-01-31T17:27:28Z
dc.date.issued2004
dc.identifier.urihttps://doi.org/10.3998/ark.5550190.0005.307
dc.identifier.urihttps://repository.tcu.edu/handle/116099117/49964
dc.description.abstractBase promoted hydrolysis of dimethyl 3aalpha,4alpha,7alpha,7aalpha-tetrahydro-4,7-methano-1H-indene-2,5-dicarboxylate (i.e., Thiele's ester, 2), performed by using KOH-MeOH, afforded after aqueous acidic workup the corresponding diacid (i.e., Thiele's acid, 1) along with a minor reaction product, 3. Compound 3 has been shown to possess structure 3a via application of single crystal X-ray crystallographic techniques.
dc.language.isoenen_US
dc.publisherSpringerNature
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceArkivoc
dc.subjectMichael addition
dc.subjectselective ester hydrolysis
dc.subjectX-ray crystal structure determination
dc.titleStructure of a minor reaction product formed via base promoted hydrolysis of Thiele's ester
dc.typeArticle
dc.rights.holderArkat Usa Inc
dc.rights.licenseCC BY 4.0
local.collegeCollege of Science and Engineering
local.departmentChemistry and Biochemistry
local.personsWatson (CHEM)


Files in this item

Thumbnail
This item appears in the following Collection(s)

Show simple item record

https://creativecommons.org/licenses/by/4.0/
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/