Iron/Copper Co-Catalyzed Cross-Coupling Reaction for the Synthesis of 6-Substituted 7-Deazapurines and the Corresponding Nucleosides-Reference-Cited by-同舟云学术

Iron/Copper Co-Catalyzed Cross-Coupling Reaction for the Synthesis of 6-Substituted 7-Deazapurines and the Corresponding Nucleosides

Published:2019-12-20 Issue:2 Volume:85 Page:403-418
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Qingfeng¹,Persoons Leentje²,Daelemans Dirk²,Herdewijn Piet¹^ORCID

Affiliation:

1. KU Leuven, Rega Institute for Medical Research, Medicinal Chemistry, Herestraat 49-bus 1041, 3000 Leuven, Belgium

2. KU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute for Medical Research, KU Leuven, Herestraat 49-bus 1043, 3000 Leuven, Belgium

Funder

KU Leuven

Fonds Wetenschappelijk Onderzoek

China Scholarship Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02414

Reference40 articles.

1. Therapeutic potential of purine analogue combinations in the treatment of lymphoid malignancies

2. Nucleoside analogues in the treatment of haematological malignancies

3. A facile synthesis of tubercidin and related 7-deazapurine nucleosides the stereospecific sodium salt glycosylation procedure

4. Pyrrolopyrimidine nucleosides. III. Total synthesis of toyocamycin, sangivamycin, tubercidin, and related derivatives

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