The synthesis of the 8-C-substituted 2,6-diamino-9-[2-(phosphonomethoxy)ethyl]purine (PMEDAP) derivatives by diverse cross-coupling reactions
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F11%3A00360763" target="_blank" >RIV/61388963:_____/11:00360763 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1139/V11-001" target="_blank" >http://dx.doi.org/10.1139/V11-001</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1139/V11-001" target="_blank" >10.1139/V11-001</a>
Alternative languages
Result language
angličtina
Original language name
The synthesis of the 8-C-substituted 2,6-diamino-9-[2-(phosphonomethoxy)ethyl]purine (PMEDAP) derivatives by diverse cross-coupling reactions
Original language description
The synthesis of the 8-C-substituted 2,6-diamino-9-[2-(phosphonomethoxy)ethyl]purine (PMEDAP) analogues was performed from diisopropyl 8-bromo-2,6-diamino-9-[2-(phosphonomethoxy)ethyl]purine using Stille, Suzuki-Miyaura, Negishi, and Sonogashira cross-coupling reactions, as well as Pd-catalysed reactions with trialkylaluminiums.
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
<a href="/en/project/1M0508" target="_blank" >1M0508: New Antivirals and Antineoplastics</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Canadian Journal of Chemistry
ISSN
0008-4042
e-ISSN
—
Volume of the periodical
89
Issue of the periodical within the volume
4
Country of publishing house
CA - CANADA
Number of pages
11
Pages from-to
488-489
UT code for WoS article
000288873200007
EID of the result in the Scopus database
—