Direct C-H borylation and C-H arylation of pyrrolo[2,3-d]pyrimidines: synthesis of 6,8-disubstituted 7-deazapurines
Organic & biomolecular chemistry.
2009 Mar 07 ;
7 (5) :
866-8.
[epub] 20090114
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid19225668
PubMed
19225668
DOI
10.1039/b900218a
Knihovny.cz E-resources
- MeSH
- Catalysis MeSH
- Purines chemical synthesis MeSH
- Pyrimidines chemistry MeSH
- Pyrroles chemistry MeSH
- Boron Compounds chemistry MeSH
- Tubercidin MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Purines MeSH
- Pyrimidines MeSH
- Pyrroles MeSH
- Boron Compounds MeSH
- Tubercidin MeSH
Novel direct C-H borylations of 7-deazapurines to position 8 by B2pin2 under Ir catalysis were followed by Suzuki cross-couplings with aryl halides and other functional group transformations to give diverse 8-substituted 7-deazaadenines.
References provided by Crossref.org
