| dc.contributor.author |
Aksu, Kadir |
|
| dc.contributor.author |
Kelebekli, Latif |
|
| dc.contributor.author |
Sahin, Ertan |
|
| dc.date.accessioned |
2022-08-17T07:11:25Z |
|
| dc.date.available |
2022-08-17T07:11:25Z |
|
| dc.date.issued |
2018 |
|
| dc.identifier.uri |
http://doi.org/10.1016/j.tetlet.2018.02.050 |
|
| dc.identifier.uri |
http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/2702 |
|
| dc.description.abstract |
The regio- and stereospecific synthesis of DL-4,5-dibromo-4,5-dideoxy-3,6-O-methyl-chiro-inositol is reported. Bromination of p-benzoquinone followed by reduction of the carbonyl groups with NaBH4 gave the corresponding trans-dibromodiol compound, which was reacted with sodium methoxide to produce dimethoxy conduritol-B. Regiospecific bromination of the alkene moiety furnished the desired chiro-inositol derivative. (C) 2018 Published by Elsevier Ltd. |
en_US |
| dc.language.iso |
eng |
en_US |
| dc.publisher |
PERGAMON-ELSEVIER SCIENCE LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND |
en_US |
| dc.relation.isversionof |
10.1016/j.tetlet.2018.02.050 |
en_US |
| dc.rights |
info:eu-repo/semantics/openAccess |
en_US |
| dc.subject |
chiro-Inositol; Methoxy conduritol-B; Methoxy inositol; Regio- and stereospecific synthesis |
en_US |
| dc.title |
Regio- and stereospecific synthesis of DL-4,5-dibromo-4,5-dideoxy-3,6-O-methyl-chiro-inositol |
en_US |
| dc.type |
article |
en_US |
| dc.relation.journal |
TETRAHEDRON LETTERS |
en_US |
| dc.contributor.department |
Ordu Üniversitesi |
en_US |
| dc.contributor.authorID |
0000-0002-6242-2589 |
en_US |
| dc.identifier.volume |
59 |
en_US |
| dc.identifier.issue |
13 |
en_US |
| dc.identifier.startpage |
1258 |
en_US |
| dc.identifier.endpage |
1260 |
en_US |