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dc.contributor.advisorCraig, Rhoda E. R., 1933-
dc.contributor.authorHombergh, Tony Vanden
dc.descriptionx, 130 p.en_US
dc.description.abstractImides and anhydrides are both important synthetic precursors to natural products, some of which have significant medical application. The current study is limited to unsymmetrically substituted anhydrides and imides having a cyclic five membered ring or bicyclic nuclei as follows: i) Anhydrides: 3-substituted 2,5-furandiones and 2-substituted bicyclo(2.2.l) heptene anhydrides having the corresponding IUPAC nomenclature of 4,7-methanoisobenzofuran-l,3- dione-3a,4,7,7a-tetrahydro- (3a α, 4 α, 7 α, 7a α) ii) Imides: 3-substituted lH-pyrrole-2,5-dione and 2-substituted bicyclo(2.2.l) heptene imides having the corresponding IUPAC nomenclature of 4,7-methano-1H-Isoindole-l,3-dione 3a,4,7,7a tetrahydro- (3a α, 4 α, 7 α, 7a α).en_US
dc.description.abstractIf you are not a current K College student, faculty, or staff member, email to request access to this SIP.
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Chemistry Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Chemistry.
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder. All rights reserved.
dc.titleSynthesis of Unsymmetrically Substituted Imides from the Corresponding 2,5-Furandiones and 5-Bicyclo(2.2.1)heptene-2,3-Carboxylic Anhydridesen_US

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