Synthesis of carba analogues of deoxy-4- C -(hydroxymethyl)hexopyranoses, intermediates in the synthesis of carbocyclic nucleosides.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F01%3A57010207" target="_blank" >RIV/61388963:_____/01:57010207 - isvavai.cz</a>
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Synthesis of carba analogues of deoxy-4- C -(hydroxymethyl)hexopyranoses, intermediates in the synthesis of carbocyclic nucleosides.
Original language description
3-O-Benzyl-1,2-O-isopropylidene-.alfa.- D -glucofuranose-5,6-O-sulfate was transformed to (1 R ,2 S ,4 R )-5,5-bis(hydroxymethyl)cyclohexane-1,2,4-triol and 3-O-benzyl-5,6-dideoxy-6-iodo-1,2-O-isopropylidene-.alfa.- D-xylo -hexofuranose was converted to(1 R ,3 R )-4,4-bis(hydroxymethyl)cyclohexane-1,3-diol.
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—
Result continuities
Project
—
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2001
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Collection of Czechoslovak Chemical Communications
ISSN
0010-0765
e-ISSN
—
Volume of the periodical
66
Issue of the periodical within the volume
5
Country of publishing house
CZ - CZECH REPUBLIC
Number of pages
14
Pages from-to
785-798
UT code for WoS article
—
EID of the result in the Scopus database
—