An Efficient Synthesis of 2-Substituted 6-Methylpurine Bases and Nucleosides by Fe- or Pd-Catalyzed Cross-Coupling Reactions of 2,6-Dichloropurines-Reference-Cited by-同舟云学术

An Efficient Synthesis of 2-Substituted 6-Methylpurine Bases and Nucleosides by Fe- or Pd-Catalyzed Cross-Coupling Reactions of 2,6-Dichloropurines

Published:2003-06-13 Issue:14 Volume:68 Page:5773-5776
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hocek Michal¹,Dvořáková Hana¹

Affiliation:

1. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, CZ-16610 Prague 6, Czech Republic. Central NMR Laboratory, Prague Institute of Chemical Technology, CZ-16628 Prague 6, Czech Republic hocek@uochb.cas.cz

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo034351i

Reference35 articles.

1. Analogs of 6-methyl-9.beta.-D-ribofuranosylpurine

2. Adenosine phosphorylase-mediated nucleoside toxicity

3. Depletion of mycoplasma from infected cell lines by limiting dilution in 6-methylpurine deoxyriboside

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