dc.contributor.author |
CONSTANTINOUKOKOTOU, V |
en |
dc.contributor.author |
COULADOUROS, EA |
en |
dc.contributor.author |
GEORGIADIS, MP |
en |
dc.contributor.author |
KOKOTOS, G |
en |
dc.date.accessioned |
2014-06-06T06:41:59Z |
|
dc.date.available |
2014-06-06T06:41:59Z |
|
dc.date.issued |
1991 |
en |
dc.identifier.issn |
0732-8303 |
en |
dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/366 |
|
dc.subject.classification |
Biochemistry & Molecular Biology |
en |
dc.subject.classification |
Chemistry, Organic |
en |
dc.subject.other |
BUILDING-BLOCKS |
en |
dc.subject.other |
DERIVATIVES |
en |
dc.subject.other |
MONOSACCHARIDES |
en |
dc.subject.other |
OXIDATION |
en |
dc.subject.other |
ALCOHOL |
en |
dc.title |
PRODUCTS FROM FURANS .12. RESOLUTION OF 2,3-DIDEOXY-DL-2-ENOPYRANOS-4-ULOSES VIA CHROMATOGRAPHIC-SEPARATION OF THEIR DIASTEREOMERIC 0-TERT-BUTYLOXYCARBONYL-L-ALANYL ESTERS - A CONVENIENT SYNTHESIS OF L-ACULOSE AND D-ACULOSE |
en |
heal.type |
journalArticle |
en |
heal.language |
English |
en |
heal.publicationDate |
1991 |
en |
heal.abstract |
A simple and effective procedure for the resolution of 2,3-dideoxy-DL-2-enopyranos-4-uloses is presented. This procedure is based on column chromatographic separation of their diastereomeric O-(N-tert-butyloxycarbonyl)-L-alanyl esters, followed by mild acidic cleavage of the ester function. L-Aculosc, 2,3,6-trideoxy-L-glycero-hex-2-enopyranos-4-ulose, is also prepared in satisfactory yield. |
en |
heal.publisher |
MARCEL DEKKER INC |
en |
heal.journalName |
JOURNAL OF CARBOHYDRATE CHEMISTRY |
en |
dc.identifier.issue |
5 |
en |
dc.identifier.volume |
10 |
en |
dc.identifier.isi |
ISI:A1991GN51900003 |
en |
dc.identifier.spage |
749 |
en |
dc.identifier.epage |
756 |
en |