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Versatile, convenient synthesis of pyrimido[1,2,3-cd]purinediones
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title
Versatile, convenient synthesis of pyrimido[1,2,3-cd]purinediones
(English)
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author name string
Stefanie Weyler
series ordinal
1
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Alaa M Hayallah
series ordinal
2
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Christa E Müller
series ordinal
3
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publication date
January 2003
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published in
Tetrahedron
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volume
59
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issue
1
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page(s)
47-54
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cites work
Imidazo[2,1-i]purin-5-ones and related tricyclic water-soluble purine derivatives: potent A(2A)- and A(3)-adenosine receptor antagonists
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7 January 2021
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7-Deazaadenines Bearing Polar Substituents: Structure−Activity Relationships of New A1and A3Adenosine Receptor Antagonists†
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7 January 2021
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Fluorescent tricyclic analogues of acyclovir and ganciclovir. A structure-antiviral activity study
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7 January 2021
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Synthesis and antiviral activity of 3-substituted derivatives of 3,9-dihydro-9-oxo-5H-imidazo[1,2-a]purines, tricyclic analogs of acyclovir and ganciclovir
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Narcotic analgesics and antagonists
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7 January 2021
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Fluorosulfonyl-substituted xanthines as selective irreversible antagonists for the A(1)-adenosine receptor
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7 January 2021
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Synthesis of paraxanthine analogs (1,7-disubstituted xanthines) and other xanthines unsubstituted at the 3-position: structure-activity relationships at adenosine receptors
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Water-soluble phosphate prodrugs of 1-propargyl-8-styrylxanthine derivatives, A(2A)-selective adenosine receptor antagonists
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7 January 2021
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1,8-disubstituted xanthine derivatives: synthesis of potent A2B-selective adenosine receptor antagonists
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7 January 2021
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Substituted 1,3-dipropylxanthines as irreversible antagonists of A1 adenosine receptors.
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7 January 2021
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Identifiers
DOI
10.1016/S0040-4020(02)01485-0
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