| dc.contributor.author |
Constantinou-Kokotou, V |
en |
| dc.contributor.author |
Couladouros, E |
en |
| dc.contributor.author |
Georgiadis, M |
en |
| dc.contributor.author |
Kokotos, G |
en |
| dc.date.accessioned |
2014-06-06T06:42:05Z |
|
| dc.date.available |
2014-06-06T06:42:05Z |
|
| dc.date.issued |
1991 |
en |
| dc.identifier.uri |
http://dx.doi.org/10.1080/07328309108543948 |
en |
| dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/412 |
|
| dc.title |
Resolution of 2,3-Dideoxy-DL-2-Enopyranos-4-Uloses Via Chromatographic Separation of their Diastereomeric O-tert-Butyloxycarbonyl-L-Alanyl Esters. A Convenient Synthesis of L- and D-Aculose |
en |
| heal.type |
journalArticle |
en |
| heal.identifier.primary |
10.1080/07328309108543948 |
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-Aculose, 2,3,6-trideoxy-L-glycero-hex-2-enopyranos-4-ulose, is also prepared in satisfactory yield. |
en |
| heal.journalName |
Journal of Carbohydrate Chemistry |
en |
| dc.identifier.doi |
10.1080/07328309108543948 |
en |