Molecular Recognition on Crystallization of Enantiopure and Racemic N-Benzoylalanine Methyl Ester

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dc.contributor.authorCoghlan, David R
dc.contributor.authorEaston, Christopher
dc.contributor.authorTiekink, Edward R
dc.date.accessioned2015-12-13T23:14:53Z
dc.date.available2015-12-13T23:14:53Z
dc.date.issued2000
dc.date.updated2015-12-12T08:40:47Z
dc.description.abstractThe melting points of crystals of (S)- and (RS)-N-benzoylalanine methyl ester derived from solutions of ethyl acetate/light petroleum are 56-57.5° and 81.5-82.5°, respectively, reflecting differences in lattice energy that are apparent from the crystal
dc.identifier.issn0004-9425
dc.identifier.urihttp://hdl.handle.net/1885/88831
dc.publisherCSIRO Publishing
dc.sourceAustralian Journal of Chemistry
dc.subjectKeywords: Amino acid methyl ester; Deuterium substitution; Enantiomeric enrichment; Supramolecular chemistry; X-ray crystal structure
dc.titleMolecular Recognition on Crystallization of Enantiopure and Racemic N-Benzoylalanine Methyl Ester
dc.typeJournal article
local.bibliographicCitation.issue7
local.bibliographicCitation.lastpage556
local.bibliographicCitation.startpage551
local.contributor.affiliationCoghlan, David R, Trinity College Dublin
local.contributor.affiliationEaston, Christopher, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationTiekink, Edward R, University of Adelaide
local.contributor.authoremailu9500570@anu.edu.au
local.contributor.authoruidEaston, Christopher, u9500570
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030505 - Physical Organic Chemistry
local.identifier.ariespublicationMigratedxPub18679
local.identifier.citationvolume53
local.identifier.scopusID2-s2.0-18744383941
local.identifier.uidSubmittedByMigrated
local.type.statusPublished Version

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