Synthesis of novel pyrazolo[3,4‐d]pyrimidines peri‐fused with 1,4‐diazepine, 1,4‐thiazepine, and 1,2,4‐triazepine rings
- 19 December 2011
- journal article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 49 (2), 315-320
- https://doi.org/10.1002/jhet.724
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Exploiting the Pyrazolo[3,4-d]pyrimidin-4-one Ring System as a Useful Template To Obtain Potent Adenosine Deaminase InhibitorsJournal of Medicinal Chemistry, 2009
- Synthesis and Antimicrobial Activity of Some New Pyrazole, Fused Pyrazolo[3,4-d]-pyrimidine and Pyrazolo[4,3-e][1,2,4]- triazolo[1,5-c]pyrimidine DerivativesMolecules, 2008
- Synthesis of a novel heterocyclic system-pyrazolo[5,4,3-de]pyrimido-[4,5-e][1,4]diazepineChemistry of Heterocyclic Compounds, 2007
- The selectivity of protein kinase inhibitors: a further updateBiochemical Journal, 2007
- Synthesis of 4-Alkynylpyrrolo[2,3-d]pyrimidines by Palladium-Catalyzed Cross-Coupling ReactionsSynthesis, 2007
- Novel, Highly Potent Adenosine Deaminase Inhibitors Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synthesis, Structure−Activity Relationships, and Molecular Modeling StudiesJournal of Medicinal Chemistry, 2005
- Palladium-Catalysed Coupling of 4-Halopyrrolo[2,3-d]pyrimidines with Arylacetylenes: Synthesis of a New Heterocyclic System - 4H-Pyrrolo[2,3,4-de]pyrimido[5′,4′:5,6][1,3]diazepino[1,7-a]indoleSynlett, 2004
- Synthesis of 3,4-diamino-1H-pyrazolo[3,4-d]pyrimidinesChemistry of Heterocyclic Compounds, 1996
- Discovery of a Novel, Potent, and Src Family-selective Tyrosine Kinase Inhibitor: STUDY OF Lck- AND FynT-DEPENDENT T CELL ACTIVATIONOnline Journal of Public Health Informatics, 1996
- Synthesis and cytotoxicity studies of 8-amino-6-methyl-2-.beta.-D-ribofuranosyl-1,2,3,5,6,7-hexaazaacenaphthylene (7-Aza-TCN) and the corresponding 2'-deoxy- and arabinonucleoside analoguesJournal of Medicinal Chemistry, 1990