Direct C-H amination and C-H chloroamination of 7-deazapurines

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F14%3A10286001" target="_blank" >RIV/00216208:11310/14:10286001 - isvavai.cz</a>
Alternative codes found
RIV/61388963:_____/14:00438287
Result on the web
<a href="http://dx.doi.org/10.1039/c4ra13143f" target="_blank" >http://dx.doi.org/10.1039/c4ra13143f</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c4ra13143f" target="_blank" >10.1039/c4ra13143f</a>

Result language
angličtina
Original language name
Direct C-H amination and C-H chloroamination of 7-deazapurines
Original language description
Protocols for selective Pd-Cu-catalyzed direct C-H amination or C-H chloroamination of 7-deazapurines with N-chloro-N-alkyl-arylsulfonamides have been developed leading either to 8-(arylsulfonyl)methylamino-7-deazapurines or to 7-chloro-8-(arylsulfonyl)methylamino-7-deazapurines. The scope and limitations of the methods, as well as synthesis of a small series of 6,8,9-tri- and 6,7,8,9-tetrasubstituted 7-deazapurines and deprotection of the sulfonamide are presented.
Czech name
—
Czech description
—

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Project
<a href="/en/project/GAP207%2F12%2F0205" target="_blank" >GAP207/12/0205: Development of novel methodologies of C-H activations of purines, deazapurines, pyrimidines and related heterocycles</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Similar results(10)